| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 114793 |
Name | FMNL2 |
Synonymous | formin-like 2;FMNL2;formin-like 2 |
Definition | formin homology 2 domain containing 2|formin homology 2 domain-containing protein 2|formin-like protein 2 |
Position | 2q23.3 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.438G>A; p.A146A; 2:152558818-152558818 |
liver | carcinoma | Substitution - coding silent |
c.1842G>A; p.V614V; 2:152625442-152625442 |
skin | malignant_melanoma | Substitution - coding silent |
c.438G>A; p.A146A; 2:152558818-152558818 |
liver | carcinoma | Substitution - coding silent |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
endometrium | carcinoma; endometrioid_carcinoma | Insertion - In frame |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
breast | carcinoma | Insertion - In frame |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
breast | carcinoma | Insertion - In frame |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
breast | carcinoma | Insertion - In frame |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1671_1672insCCA; p.P573_L574insP; 2:152619552-152619553 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1699C>T; p.P567S; 2:152619580-152619580 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1701G>A; p.P567P; 2:152619582-152619582 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1701G>A; p.P567P; 2:152619582-152619582 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1942G>A; p.D648N; 2:152625542-152625542 |
skin | malignant_melanoma | Substitution - Missense |
c.1795G>A; p.G599R; 2:152619676-152619676 |
skin | malignant_melanoma | Substitution - Missense |
c.1050C>T; p.D350D; 2:152611593-152611593 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2576G>T; p.R859I; 2:152632033-152632033 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1698A>C; p.P566P; 2:152619579-152619579 |
thyroid | other; neoplasm | Substitution - coding silent |
c.858A>G; p.A286A; 2:152581031-152581031 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1561G>A; p.A521T; 2:152619092-152619092 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.645G>T; p.V215V; 2:152575184-152575184 |
skin | malignant_melanoma | Substitution - coding silent |
c.1281C>G; p.L427L; 2:152617159-152617159 |
breast | carcinoma | Substitution - coding silent |
c.3228C>T; p.R1076R; 2:152647854-152647854 |
breast | carcinoma | Substitution - coding silent |
c.2338C>A; p.Q780K; 2:152628471-152628471 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2325C>T; p.I775I; 2:152628458-152628458 |
skin | malignant_melanoma | Substitution - coding silent |
c.675C>G; p.I225M; 2:152575214-152575214 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2325C>T; p.I775I; 2:152628458-152628458 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2659T>C; p.Y887H; 2:152632116-152632116 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2744G>A; p.R915K; 2:152636490-152636490 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.344G>T; p.R115I; 2:152549082-152549082 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2261G>A; p.R754Q; 2:152628394-152628394 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1080G>C; p.E360D; 2:152614868-152614868 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.597-1G>A; p.?; 2:152575135-152575135 |
stomach | carcinoma; intestinal_adenocarcinoma | Unknown |
c.2213G>A; p.R738Q; 2:152628346-152628346 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2772G>A; p.T924T; 2:152636518-152636518 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3047C>T; p.S1016F; 2:152640792-152640792 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.319C>A; p.L107I; 2:152549057-152549057 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1753C>T; p.P585S; 2:152619634-152619634 |
skin | malignant_melanoma | Substitution - Missense |
c.420C>T; p.L140L; 2:152558800-152558800 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1865C>G; p.T622R; 2:152625465-152625465 |
liver | carcinoma | Substitution - Missense |
c.1865C>G; p.T622R; 2:152625465-152625465 |
liver | carcinoma | Substitution - Missense |
c.1851G>A; p.K617K; 2:152625451-152625451 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2946G>T; p.K982N; 2:152637674-152637674 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2540G>A; p.S847N; 2:152629895-152629895 |
skin | malignant_melanoma | Substitution - Missense |
c.1485A>C; p.P495P; 2:152619016-152619016 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.611C>T; p.P204L; 2:152575150-152575150 |
pancreas | carcinoma | Substitution - Missense |
c.2357C>T; p.A786V; 2:152628490-152628490 |
skin | malignant_melanoma | Substitution - Missense |
c.2992C>T; p.L998F; 2:152640003-152640003 |
breast | carcinoma | Substitution - Missense |
c.3221G>T; p.R1074M; 2:152647847-152647847 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1788G>T; p.P596P; 2:152619669-152619669 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1183G>A; p.V395M; 2:152614971-152614971 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.121G>A; p.A41T; 2:152521946-152521946 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1308C>T; p.V436V; 2:152617186-152617186 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.99G>A; p.E33E; 2:152335702-152335702 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1665_1666insACC; p.P555_P556insT; 2:152619546-152619547 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; mantle_cell_lymphoma | Insertion - In frame |
c.2299C>T; p.R767W; 2:152628432-152628432 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.504G>A; p.W168*; 2:152560943-152560943 |
skin | malignant_melanoma | Substitution - Nonsense |
c.3251C>T; p.S1084F; 2:152647877-152647877 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; peripheral_T_cell_lymphoma_unspecified | Substitution - Missense |
c.1837+1G>A; p.?; 2:152619719-152619719 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Unknown |
c.1423C>A; p.L475I; 2:152618954-152618954 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1355G>T; p.R452I; 2:152618886-152618886 |
breast | carcinoma | Substitution - Missense |
c.1603C>T; p.P535S; 2:152619134-152619134 |
skin | malignant_melanoma | Substitution - Missense |
c.130C>T; p.L44L; 2:152521955-152521955 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.571C>T; p.R191C; 2:152561010-152561010 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.571C>T; p.R191C; 2:152561010-152561010 |
breast | carcinoma | Substitution - Missense |
c.1604C>T; p.P535L; 2:152619135-152619135 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2839G>A; p.A947T; 2:152636585-152636585 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.227C>T; p.P76L; 2:152542764-152542764 |
skin | malignant_melanoma | Substitution - Missense |
c.1952G>A; p.R651Q; 2:152625552-152625552 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1952G>A; p.R651Q; 2:152625552-152625552 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1753C>G; p.P585A; 2:152619634-152619634 |
liver | carcinoma | Substitution - Missense |
c.43A>G; p.R15G; 2:152335646-152335646 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1763C>A; p.A588E; 2:152619644-152619644 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.1952G>A; p.R651Q; 2:152625552-152625552 |
skin | malignant_melanoma | Substitution - Missense |
c.1123_1124insT; p.D377fs*1; 2:152614911-152614912 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1710G>C; p.P570P; 2:152619591-152619591 |
thyroid | other; neoplasm | Substitution - coding silent |
c.1677T>C; p.P559P; 2:152619558-152619558 |
lung | carcinoid-endocrine_tumour; typical | Substitution - coding silent |
c.62T>C; p.L21S; 2:152335665-152335665 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1677T>C; p.P559P; 2:152619558-152619558 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.1677T>C; p.P559P; 2:152619558-152619558 |
thyroid | other; neoplasm | Substitution - coding silent |
c.1177G>C; p.E393Q; 2:152614965-152614965 |
upper_aerodigestive_tract; larynx | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2214G>C; p.R738R; 2:152628347-152628347 |
skin | malignant_melanoma | Substitution - coding silent |
c.1213-1G>A; p.?; 2:152617090-152617090 |
endometrium | carcinoma; endometrioid_carcinoma | Unknown |
c.206G>A; p.R69Q; 2:152542743-152542743 |
skin | malignant_melanoma | Substitution - Missense |
c.157C>T; p.R53W; 2:152521982-152521982 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1312C>T; p.R438W; 2:152617190-152617190 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.180A>G; p.K60K; 2:152522005-152522005 |
soft_tissue; blood_vessel | angiosarcoma | Substitution - coding silent |
c.3136G>A; p.G1046R; 2:152640881-152640881 |
skin | malignant_melanoma | Substitution - Missense |
c.2650G>T; p.E884*; 2:152632107-152632107 |
pancreas | carcinoma | Substitution - Nonsense |
c.614G>A; p.S205N; 2:152575153-152575153 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.721G>A; p.V241I; 2:152578903-152578903 |
skin | malignant_melanoma | Substitution - Missense |
c.241C>G; p.Q81E; 2:152542778-152542778 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1256A>C; p.K419T; 2:152617134-152617134 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1686T>A; p.P562P; 2:152619567-152619567 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.733C>G; p.P245A; 2:152578915-152578915 |
breast | carcinoma | Substitution - Missense |
c.268G>A; p.A90T; 2:152542805-152542805 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.479G>A; p.S160N; 2:152560918-152560918 |
skin | malignant_melanoma | Substitution - Missense |
c.2944A>G; p.K982E; 2:152637672-152637672 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1437G>A; p.G479G; 2:152618968-152618968 |
skin | malignant_melanoma | Substitution - coding silent |
c.265C>T; p.P89S; 2:152542802-152542802 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1473C>T; p.I491I; 2:152619004-152619004 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1281C>A; p.L427L; 2:152617159-152617159 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1671G>A; p.P557P; 2:152619552-152619552 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1607C>T; p.S536L; 2:152619138-152619138 |
skin | malignant_melanoma | Substitution - Missense |
c.1607C>T; p.S536L; 2:152619138-152619138 |
skin | malignant_melanoma | Substitution - Missense |
c.1579C>T; p.P527S; 2:152619110-152619110 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1661_1662insAGC; p.P554_P555insA; 2:152619542-152619543 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; mantle_cell_lymphoma | Insertion - In frame |
c.540C>A; p.N180K; 2:152560979-152560979 |
bone; femur | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.1560C>T; p.A520A; 2:152619091-152619091 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; peripheral_T_cell_lymphoma_unspecified | Substitution - coding silent |
c.2374G>A; p.A792T; 2:152628507-152628507 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1560C>T; p.A520A; 2:152619091-152619091 |
bone; femur | chondrosarcoma | Substitution - coding silent |
c.1984G>C; p.E662Q; 2:152626546-152626546 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.594G>T; p.L198L; 2:152561033-152561033 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1707T>C; p.P569P; 2:152619588-152619588 |
thyroid | other; neoplasm | Substitution - coding silent |
c.1060G>A; p.D354N; 2:152611603-152611603 |
skin | malignant_melanoma | Substitution - Missense |
c.1209T>A; p.S403S; 2:152614997-152614997 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - coding silent |
c.2575A>G; p.R859G; 2:152632032-152632032 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2575A>G; p.R859G; 2:152632032-152632032 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2814G>A; p.K938K; 2:152636560-152636560 |
pancreas | carcinoma | Substitution - coding silent |
c.1850A>G; p.K617R; 2:152625450-152625450 |
skin | malignant_melanoma | Substitution - Missense |
c.3265G>A; p.E1089K; 2:152647891-152647891 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1817T>C; p.V606A; 2:152619698-152619698 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1565C>T; p.S522F; 2:152619096-152619096 |
skin | malignant_melanoma | Substitution - Missense |
c.1565C>T; p.S522F; 2:152619096-152619096 |
skin | malignant_melanoma | Substitution - Missense |
c.1088A>C; p.K363T; 2:152614876-152614876 |
breast | carcinoma | Substitution - Missense |
c.2524G>A; p.G842R; 2:152629879-152629879 |
skin | malignant_melanoma | Substitution - Missense |
c.834C>T; p.G278G; 2:152581007-152581007 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2742G>A; p.K914K; 2:152636488-152636488 |
skin | malignant_melanoma | Substitution - coding silent |
c.1114C>A; p.L372M; 2:152614902-152614902 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2377G>T; p.E793*; 2:152628510-152628510 |
ovary | carcinoma; serous_carcinoma | Substitution - Nonsense |
c.331G>A; p.E111K; 2:152549069-152549069 |
skin | malignant_melanoma | Substitution - Missense |
c.733C>T; p.P245S; 2:152578915-152578915 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.331G>A; p.E111K; 2:152549069-152549069 |
skin | malignant_melanoma | Substitution - Missense |
c.733C>T; p.P245S; 2:152578915-152578915 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.659A>C; p.D220A; 2:152575198-152575198 |
soft_tissue; striated_muscle | rhabdomyosarcoma; embryonal | Substitution - Missense |
c.3053C>T; p.S1018F; 2:152640798-152640798 |
breast | carcinoma | Substitution - Missense |
c.883G>A; p.G295R; 2:152607345-152607345 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1558G>A; p.A520T; 2:152619089-152619089 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2617G>T; p.E873*; 2:152632074-152632074 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.766A>T; p.N256Y; 2:152578948-152578948 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1062C>T; p.D354D; 2:152611605-152611605 |
pancreas | carcinoma | Substitution - coding silent |
c.2626C>T; p.H876Y; 2:152632083-152632083 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1756C>T; p.P586S; 2:152619637-152619637 |
skin | malignant_melanoma | Substitution - Missense |
c.2553C>G; p.L851L; 2:152632010-152632010 |
breast | carcinoma | Substitution - coding silent |
c.2576G>A; p.R859K; 2:152632033-152632033 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.3225G>C; p.R1075R; 2:152647851-152647851 |
liver | carcinoma | Substitution - coding silent |
c.2576G>A; p.R859K; 2:152632033-152632033 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1718C>T; p.P573L; 2:152619599-152619599 |
skin; trunk | malignant_melanoma | Substitution - Missense |
c.1866G>A; p.T622T; 2:152625466-152625466 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.480C>T; p.S160S; 2:152560919-152560919 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.2725G>T; p.G909*; 2:152636471-152636471 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.444-2A>T; p.?; 2:152560881-152560881 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Unknown |
c.2518G>A; p.V840I; 2:152629873-152629873 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2925C>T; p.V975V; 2:152637653-152637653 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2412G>A; p.A804A; 2:152629667-152629667 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1701G>C; p.P567P; 2:152619582-152619582 |
thyroid | other; neoplasm | Substitution - coding silent |
c.1343T>C; p.V448A; 2:152618874-152618874 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.545C>T; p.P182L; 2:152560984-152560984 |
skin | malignant_melanoma | Substitution - Missense |
c.714C>A; p.F238L; 2:152578896-152578896 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1674C>A; p.P558P; 2:152619555-152619555 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1674C>A; p.P558P; 2:152619555-152619555 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1674C>A; p.P558P; 2:152619555-152619555 |
lung | carcinoid-endocrine_tumour; typical | Substitution - coding silent |
c.1674C>A; p.P558P; 2:152619555-152619555 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.1674C>A; p.P558P; 2:152619555-152619555 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1674C>A; p.P558P; 2:152619555-152619555 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.617G>A; p.R206K; 2:152575156-152575156 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2151T>C; p.C717C; 2:152626713-152626713 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.923G>A; p.R308K; 2:152607385-152607385 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2458A>G; p.K820E; 2:152629713-152629713 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.110_111delTC; p.I37fs*10; 2:152335713-152335714 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Deletion - Frameshift |
c.1405G>A; p.E469K; 2:152618936-152618936 |
skin | malignant_melanoma | Substitution - Missense |
c.2442G>A; p.S814S; 2:152629697-152629697 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2050C>A; p.P684T; 2:152626612-152626612 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.620G>T; p.R207I; 2:152575159-152575159 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2050C>A; p.P684T; 2:152626612-152626612 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2267G>A; p.R756K; 2:152628400-152628400 |
skin | malignant_melanoma | Substitution - Missense |
c.3227G>A; p.R1076H; 2:152647853-152647853 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1476C>T; p.A492A; 2:152619007-152619007 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1623A>C; p.E541D; 2:152619154-152619154 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |