| Gene ID | 10568 |
| Symbol | SLC34A2 |
| Synonymous | NAPI-3B|NAPI-IIb|NPTIIb |
| Full name | solute carrier family 34 (type II sodium/phosphate cotransporter), member 2 |
| Gene description | sodium-dependent phosphate transport protein 2B|sodium/phosphate cotransporter 2B|solute carrier family 34 (sodium phosphate), member 2|type II sodium-dependent phosphate transporter 3b |
| Cytoband | 4p15.2 |
| Gene type | protein-coding |
| Synonymous | MIM:604217; HGNC:HGNC:11020; Ensembl:ENSG00000157765; HPRD:07251; Vega:OTTHUMG00000097757 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1551G>A; p.G517G; 4:25676227-25676227 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.66A>G; p.A22A; 4:25662566-25662566 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.1883C>T; p.A628V; 4:25676559-25676559 |
breast | carcinoma | Substitution - Missense |
c.479C>G; p.S160C; 4:25666227-25666227 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.521C>T; p.S174L; 4:25666269-25666269 |
skin | malignant_melanoma | Substitution - Missense |
c.1264G>T; p.V422F; 4:25674343-25674343 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.861A>G; p.A287A; 4:25670767-25670767 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.7C>T; p.P3S; 4:25662507-25662507 |
skin | malignant_melanoma | Substitution - Missense |
c.1936G>A; p.E646K; 4:25676612-25676612 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1755G>T; p.K585N; 4:25676431-25676431 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1639C>T; p.L547F; 4:25676315-25676315 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1849C>T; p.R617C; 4:25676525-25676525 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1872_1883delGTGCTGCCGCGC; p.R627_C630delRACC; 4:25676548-25676559 |
breast | carcinoma | Deletion - In frame |
c.1373C>T; p.T458M; 4:25674544-25674544 |
pancreas | carcinoma | Substitution - Missense |
c.112+10G>A; p.?; 4:25662622-25662622 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Unknown |
c.397T>C; p.F133L; 4:25666145-25666145 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1751C>T; p.P584L; 4:25676427-25676427 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.991G>A; p.D331N; 4:25671664-25671664 |
skin | malignant_melanoma | Substitution - Missense |
c.1221C>T; p.F407F; 4:25674300-25674300 |
skin; neck | malignant_melanoma | Substitution - coding silent |
c.1221C>T; p.F407F; 4:25674300-25674300 |
skin | malignant_melanoma | Substitution - coding silent |
c.1764G>A; p.Q588Q; 4:25676440-25676440 |
skin | malignant_melanoma | Substitution - coding silent |
c.1945G>A; p.E649K; 4:25676621-25676621 |
skin | malignant_melanoma | Substitution - Missense |
c.1945G>A; p.E649K; 4:25676621-25676621 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.270G>T; p.K90N; 4:25664221-25664221 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1239G>A; p.W413*; 4:25674318-25674318 |
skin | malignant_melanoma | Substitution - Nonsense |
c.2043G>A; p.S681S; 4:25676719-25676719 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2043G>A; p.S681S; 4:25676719-25676719 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1008G>A; p.W336*; 4:25671681-25671681 |
skin | malignant_melanoma | Substitution - Nonsense |
c.202G>A; p.D68N; 4:25662794-25662794 |
skin | malignant_melanoma | Substitution - Missense |
c.1042G>T; p.A348S; 4:25671715-25671715 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.855A>G; p.Q285Q; 4:25670761-25670761 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1402A>G; p.T468A; 4:25674573-25674573 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1402A>G; p.T468A; 4:25674573-25674573 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.989C>T; p.T330M; 4:25671662-25671662 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.1800G>A; p.L600L; 4:25676476-25676476 |
skin | malignant_melanoma | Substitution - coding silent |
c.762C>T; p.F254F; 4:25669773-25669773 |
breast | carcinoma | Substitution - coding silent |
c.1032G>A; p.K344K; 4:25671705-25671705 |
skin | malignant_melanoma | Substitution - coding silent |
c.1389C>T; p.I463I; 4:25674560-25674560 |
skin | malignant_melanoma | Substitution - coding silent |
c.1518G>A; p.P506P; 4:25676194-25676194 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.42C>A; p.P14P; 4:25662542-25662542 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.303G>A; p.L101L; 4:25664254-25664254 |
skin | malignant_melanoma | Substitution - coding silent |
c.1284C>A; p.F428L; 4:25674363-25674363 |
breast | carcinoma | Substitution - Missense |
c.828C>T; p.V276V; 4:25669839-25669839 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1651G>T; p.G551C; 4:25676327-25676327 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1510C>T; p.P504S; 4:25676186-25676186 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1593C>G; p.F531L; 4:25676269-25676269 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1517C>G; p.P506R; 4:25676193-25676193 |
skin | malignant_melanoma | Substitution - Missense |
c.928A>G; p.T310A; 4:25671601-25671601 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1311G>A; p.T437T; 4:25674390-25674390 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1107C>G; p.L369L; 4:25673145-25673145 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.662A>T; p.D221V; 4:25669673-25669673 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1630G>A; p.V544M; 4:25676306-25676306 |
skin | malignant_melanoma | Substitution - Missense |
c.1563C>A; p.I521I; 4:25676239-25676239 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.54C>T; p.L18L; 4:25662554-25662554 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1919G>A; p.R640H; 4:25676595-25676595 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1115C>T; p.S372F; 4:25673153-25673153 |
skin | malignant_melanoma | Substitution - Missense |
c.1675G>T; p.G559W; 4:25676351-25676351 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.770G>C; p.G257A; 4:25669781-25669781 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1717C>T; p.R573*; 4:25676393-25676393 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.1819G>A; p.V607I; 4:25676495-25676495 |
bone; scapula | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.1819G>A; p.V607I; 4:25676495-25676495 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |
c.747G>T; p.V249V; 4:25669758-25669758 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.829C>T; p.Q277*; 4:25669840-25669840 |
skin | malignant_melanoma | Substitution - Nonsense |
c.1205C>A; p.T402N; 4:25673243-25673243 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.315C>T; p.L105L; 4:25664266-25664266 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1575T>A; p.Y525*; 4:25676251-25676251 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1185C>T; p.V395V; 4:25673223-25673223 |
skin | malignant_melanoma | Substitution - coding silent |
c.1313C>T; p.S438L; 4:25674392-25674392 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1657C>T; p.R553W; 4:25676333-25676333 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1575delT; p.R526fs*8; 4:25676251-25676251 |
lung | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1752G>A; p.P584P; 4:25676428-25676428 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1752G>A; p.P584P; 4:25676428-25676428 |
skin | malignant_melanoma | Substitution - coding silent |
c.771A>G; p.G257G; 4:25669782-25669782 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.771A>G; p.G257G; 4:25669782-25669782 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1776C>T; p.F592F; 4:25676452-25676452 |
skin | malignant_melanoma | Substitution - coding silent |
c.296G>T; p.G99V; 4:25664247-25664247 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.380_381insA; p.M129fs*81; 4:25666128-25666129 |
oesophagus | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1650C>T; p.A550A; 4:25676326-25676326 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_B_cell_leukaemia | Substitution - coding silent |
c.966C>T; p.C322C; 4:25671639-25671639 |
bone; femur | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.322C>A; p.L108I; 4:25664273-25664273 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1588G>A; p.V530I; 4:25676264-25676264 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1156A>T; p.I386F; 4:25673194-25673194 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1627A>T; p.T543S; 4:25676303-25676303 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1816G>A; p.V606I; 4:25676492-25676492 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1018A>T; p.N340Y; 4:25671691-25671691 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.203A>G; p.D68G; 4:25662795-25662795 |
breast | carcinoma | Substitution - Missense |
c.442G>A; p.V148M; 4:25666190-25666190 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.447C>A; p.I149I; 4:25666195-25666195 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1884G>A; p.A628A; 4:25676560-25676560 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.754T>G; p.F252V; 4:25669765-25669765 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1806C>T; p.P602P; 4:25676482-25676482 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1884G>A; p.A628A; 4:25676560-25676560 |
liver | carcinoma | Substitution - coding silent |
c.1683C>T; p.P561P; 4:25676359-25676359 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1683C>T; p.P561P; 4:25676359-25676359 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.990G>A; p.T330T; 4:25671663-25671663 |
skin | malignant_melanoma | Substitution - coding silent |
c.769G>T; p.G257*; 4:25669780-25669780 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1287C>T; p.I429I; 4:25674366-25674366 |
skin | malignant_melanoma | Substitution - coding silent |
c.572G>C; p.G191A; 4:25667928-25667928 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.765G>A; p.K255K; 4:25669776-25669776 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.137C>T; p.T46I; 4:25662729-25662729 |
breast | carcinoma | Substitution - Missense |
c.765G>A; p.K255K; 4:25669776-25669776 |
skin | malignant_melanoma | Substitution - coding silent |
c.1614C>T; p.F538F; 4:25676290-25676290 |
skin | malignant_melanoma | Substitution - coding silent |
c.1340G>A; p.G447D; 4:25674511-25674511 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1614C>T; p.F538F; 4:25676290-25676290 |
skin | malignant_melanoma | Substitution - coding silent |
c.1865G>C; p.C622S; 4:25676541-25676541 |
pancreas | carcinoma | Substitution - Missense |
c.591T>C; p.T197T; 4:25667947-25667947 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.374T>C; p.V125A; 4:25664325-25664325 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.1659G>A; p.R553R; 4:25676335-25676335 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.592A>T; p.I198F; 4:25667948-25667948 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1938G>T; p.E646D; 4:25676614-25676614 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.282C>A; p.F94L; 4:25664233-25664233 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.183T>A; p.D61E; 4:25662775-25662775 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.333C>T; p.F111F; 4:25664284-25664284 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.333C>T; p.F111F; 4:25664284-25664284 |
skin; hand | malignant_melanoma | Substitution - coding silent |
c.333C>T; p.F111F; 4:25664284-25664284 |
pancreas | carcinoma; ductal_carcinoma | Substitution - coding silent |
c.333C>T; p.F111F; 4:25664284-25664284 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.333C>T; p.F111F; 4:25664284-25664284 |
skin | malignant_melanoma | Substitution - coding silent |
c.28G>A; p.A10T; 4:25662528-25662528 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1742G>A; p.R581H; 4:25676418-25676418 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1952C>T; p.A651V; 4:25676628-25676628 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1952C>T; p.A651V; 4:25676628-25676628 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1952C>T; p.A651V; 4:25676628-25676628 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1585G>A; p.A529T; 4:25676261-25676261 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1842C>T; p.F614F; 4:25676518-25676518 |
skin; arm | malignant_melanoma | Substitution - coding silent |
c.1538G>A; p.R513H; 4:25676214-25676214 |
breast | carcinoma | Substitution - Missense |
c.1849_1850insGCT; p.C622_R623insC; 4:25676525-25676526 |
large_intestine; caecum | carcinoma; adenocarcinoma | Insertion - In frame |
c.1207A>G; p.I403V; 4:25673245-25673245 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.979C>T; p.L327F; 4:25671652-25671652 |
skin | malignant_melanoma | Substitution - Missense |
c.1011C>T; p.T337T; 4:25671684-25671684 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1739C>T; p.P580L; 4:25676415-25676415 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.870T>C; p.D290D; 4:25670776-25670776 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1864_1866delTGC; p.C622delC; 4:25676540-25676542 |
endometrium | carcinoma; serous_carcinoma | Deletion - In frame |
c.2029G>A; p.E677K; 4:25676705-25676705 |
skin | malignant_melanoma | Substitution - Missense |
c.1462G>T; p.A488S; 4:25676138-25676138 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1779G>A; p.L593L; 4:25676455-25676455 |
lung | carcinoma; small_cell_carcinoma | Substitution - coding silent |
c.1834G>A; p.G612S; 4:25676510-25676510 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1228C>T; p.P410S; 4:25674307-25674307 |
skin | malignant_melanoma | Substitution - Missense |
c.1621C>T; p.P541S; 4:25676297-25676297 |
skin; trunk | malignant_melanoma; nodular | Substitution - Missense |
c.555C>T; p.I185I; 4:25667911-25667911 |
skin | malignant_melanoma | Substitution - coding silent |
c.621G>A; p.R207R; 4:25667977-25667977 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1792C>T; p.R598C; 4:25676468-25676468 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.8C>T; p.P3L; 4:25662508-25662508 |
skin | malignant_melanoma | Substitution - Missense |
c.2056G>A; p.E686K; 4:25676732-25676732 |
skin | malignant_melanoma | Substitution - Missense |
c.741_742delTA; p.I248fs*21; 4:25669752-25669753 |
lung | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1255G>T; p.A419S; 4:25674334-25674334 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1486A>T; p.I496F; 4:25676162-25676162 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.1850_1855delGCTGCT; p.C621_C622delCC; 4:25676526-25676531 |
ovary | carcinoma; serous_carcinoma | Deletion - In frame |
c.492G>A; p.T164T; 4:25666240-25666240 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2027G>A; p.G676D; 4:25676703-25676703 |
skin | malignant_melanoma | Substitution - Missense |
c.1417G>A; p.A473T; 4:25674588-25674588 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.204C>T; p.D68D; 4:25662796-25662796 |
liver | carcinoma | Substitution - coding silent |
c.1637G>A; p.G546D; 4:25676313-25676313 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.193G>A; p.E65K; 4:25662785-25662785 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.266G>A; p.G89E; 4:25664217-25664217 |
skin | malignant_melanoma | Substitution - Missense |
c.40C>T; p.P14S; 4:25662540-25662540 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1451C>T; p.S484L; 4:25674622-25674622 |
skin | malignant_melanoma | Substitution - Missense |
c.43G>A; p.D15N; 4:25662543-25662543 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.43G>A; p.D15N; 4:25662543-25662543 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1606T>A; p.F536I; 4:25676282-25676282 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2044G>A; p.D682N; 4:25676720-25676720 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1229C>T; p.P410L; 4:25674308-25674308 |
skin | malignant_melanoma | Substitution - Missense |
c.835G>A; p.D279N; 4:25670741-25670741 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1516C>T; p.P506S; 4:25676192-25676192 |
skin | malignant_melanoma | Substitution - Missense |
c.30C>T; p.A10A; 4:25662530-25662530 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1491C>T; p.S497S; 4:25676167-25676167 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1814C>A; p.A605D; 4:25676490-25676490 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.486C>A; p.T162T; 4:25666234-25666234 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1620C>G; p.I540M; 4:25676296-25676296 |
skin | malignant_melanoma | Substitution - Missense |
c.1122G>T; p.L374L; 4:25673160-25673160 |
lung | carcinoma; small_cell_carcinoma | Substitution - coding silent |
c.585C>A; p.T195T; 4:25667941-25667941 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1783C>A; p.L595M; 4:25676459-25676459 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1687G>A; p.V563I; 4:25676363-25676363 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1674C>T; p.V558V; 4:25676350-25676350 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1687G>A; p.V563I; 4:25676363-25676363 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.721C>T; p.L241F; 4:25669732-25669732 |
skin | malignant_melanoma | Substitution - Missense |
c.721C>T; p.L241F; 4:25669732-25669732 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.975T>G; p.P325P; 4:25671648-25671648 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1922G>T; p.C641F; 4:25676598-25676598 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1461C>T; p.I487I; 4:25676137-25676137 |
skin | malignant_melanoma | Substitution - coding silent |
c.1732C>T; p.R578C; 4:25676408-25676408 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2063C>T; p.T688M; 4:25676739-25676739 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1461C>T; p.I487I; 4:25676137-25676137 |
skin | malignant_melanoma | Substitution - coding silent |
c.1732C>T; p.R578C; 4:25676408-25676408 |
skin | malignant_melanoma | Substitution - Missense |
c.2063C>T; p.T688M; 4:25676739-25676739 |
thyroid | carcinoma | Substitution - Missense |
c.1665G>C; p.L555L; 4:25676341-25676341 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1542G>A; p.M514I; 4:25676218-25676218 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1611C>T; p.F537F; 4:25676287-25676287 |
lung | carcinoma; small_cell_carcinoma | Substitution - coding silent |
c.19T>A; p.L7M; 4:25662519-25662519 |
skin | malignant_melanoma | Substitution - Missense |
c.535C>T; p.R179W; 4:25667891-25667891 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1453C>G; p.L485V; 4:25674624-25674624 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.1488C>T; p.I496I; 4:25676164-25676164 |
liver | carcinoma | Substitution - coding silent |
c.2067C>T; p.A689A; 4:25676743-25676743 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1077C>T; p.L359L; 4:25673115-25673115 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1113C>T; p.L371L; 4:25673151-25673151 |
skin | malignant_melanoma | Substitution - coding silent |
c.1301C>A; p.S434Y; 4:25674380-25674380 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1628C>T; p.T543M; 4:25676304-25676304 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.290G>A; p.G97E; 4:25664241-25664241 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1550G>T; p.G517V; 4:25676226-25676226 |
thyroid | other; neoplasm | Substitution - Missense |
c.290G>A; p.G97E; 4:25664241-25664241 |
skin | malignant_melanoma | Substitution - Missense |
c.1041C>T; p.I347I; 4:25671714-25671714 |
skin | malignant_melanoma | Substitution - coding silent |
c.699C>T; p.P233P; 4:25669710-25669710 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.693C>T; p.L231L; 4:25669704-25669704 |
prostate | adenoma | Substitution - coding silent |
c.750G>T; p.E250D; 4:25669761-25669761 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |