| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 6714 |
Name | SRC |
Synonymous | SRC proto-oncogene, non-receptor tyrosine kinase;SRC;SRC proto-oncogene, non-receptor tyrosine kinase |
Definition | proto-oncogene c-Src|proto-oncogene tyrosine-protein kinase Src|protooncogene SRC, Rous sarcoma|tyrosine kinase pp60c-src|tyrosine-protein kinase SRC-1|v-src avian sarcoma (Schmidt-Ruppin A-2) viral oncogene homolog |
Position | 20q12-q13 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1282C>A; p.P428T; 20:37402760-37402760 |
biliary_tract; gallbladder | carcinoma; adenocarcinoma | Substitution - Missense |
c.870C>T; p.N290N; 20:37400125-37400125 |
breast | carcinoma | Substitution - coding silent |
c.651C>T; p.I217I; 20:37396259-37396259 |
breast | carcinoma | Substitution - coding silent |
c.806C>T; p.S269L; 20:37397801-37397801 |
breast | carcinoma | Substitution - Missense |
c.1040G>A; p.G347E; 20:37401602-37401602 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1040G>A; p.G347E; 20:37401602-37401602 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.832C>G; p.Q278E; 20:37397827-37397827 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.90C>T; p.G30G; 20:37384243-37384243 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.759G>A; p.P253P; 20:37397754-37397754 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.361T>C; p.W121R; 20:37393905-37393905 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1021A>G; p.T341A; 20:37400276-37400276 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1591C>T; p.Q531*; 20:37403359-37403359 |
endometrium | carcinoma | Substitution - Nonsense |
c.397G>T; p.G133C; 20:37393941-37393941 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.272C>T; p.A91V; 20:37386096-37386096 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.423G>A; p.A141A; 20:37393967-37393967 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.591C>A; p.A197A; 20:37396199-37396199 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.926C>T; p.A309V; 20:37400181-37400181 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.756G>T; p.K252N; 20:37397751-37397751 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.631G>A; p.D211N; 20:37396239-37396239 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.681G>A; p.Q227Q; 20:37396289-37396289 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.813G>A; p.R271R; 20:37397808-37397808 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1138G>A; p.V380M; 20:37402456-37402456 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.421G>A; p.A141T; 20:37393965-37393965 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.588C>T; p.N196N; 20:37396196-37396196 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.337A>T; p.I113F; 20:37386161-37386161 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.337A>T; p.I113F; 20:37386161-37386161 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1018G>A; p.V340I; 20:37400273-37400273 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.6T>G; p.G2G; 20:37384159-37384159 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.767_768delAG; p.Q256fs*67; 20:37397762-37397763 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.767_768delAG; p.Q256fs*67; 20:37397762-37397763 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.636C>T; p.S212S; 20:37396244-37396244 |
large_intestine; colon | NS | Substitution - coding silent |
c.1081C>A; p.L361M; 20:37401643-37401643 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.750G>A; p.T250T; 20:37397745-37397745 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1219G>A; p.D407N; 20:37402537-37402537 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1571C>T; p.T524M; 20:37403339-37403339 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1460C>T; p.P487L; 20:37403228-37403228 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1591C>T; p.Q531*; 20:37403359-37403359 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1591C>T; p.Q531*; 20:37403359-37403359 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1591C>T; p.Q531*; 20:37403359-37403359 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1591C>T; p.Q531*; 20:37403359-37403359 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1591C>T; p.Q531*; 20:37403359-37403359 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1591C>T; p.Q531*; 20:37403359-37403359 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1591C>T; p.Q531*; 20:37403359-37403359 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1591C>T; p.Q531*; 20:37403359-37403359 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1591C>T; p.Q531*; 20:37403359-37403359 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1591C>T; p.Q531*; 20:37403359-37403359 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1261G>T; p.A421S; 20:37402579-37402579 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.423G>T; p.A141A; 20:37393967-37393967 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1155C>T; p.Y385Y; 20:37402473-37402473 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.51C>T; p.S17S; 20:37384204-37384204 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.330G>A; p.R110R; 20:37386154-37386154 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.423G>A; p.A141A; 20:37393967-37393967 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.423G>A; p.A141A; 20:37393967-37393967 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.464A>G; p.K155R; 20:37394188-37394188 |
liver | carcinoma | Substitution - Missense |
c.405C>T; p.I135I; 20:37393949-37393949 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1402+1G>T; p.?; 20:37402881-37402881 |
lung | carcinoma; adenocarcinoma | Unknown |
c.363G>T; p.W121C; 20:37393907-37393907 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.736A>T; p.T246S; 20:37397731-37397731 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1022C>G; p.T341R; 20:37400277-37400277 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.250+6T>G; p.?; 20:37384409-37384409 |
NS | NS | Unknown |
c.1262C>T; p.A421V; 20:37402580-37402580 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.411C>T; p.S137S; 20:37393955-37393955 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.1219G>C; p.D407H; 20:37402537-37402537 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1579G>A; p.E527K; 20:37403347-37403347 |
pancreas | carcinoma | Substitution - Missense |
c.1579G>A; p.E527K; 20:37403347-37403347 |
pancreas | carcinoma | Substitution - Missense |
c.703+10C>T; p.?; 20:37396321-37396321 |
pancreas | carcinoma | Unknown |
c.346A>G; p.N116D; 20:37386170-37386170 |
prostate | carcinoma | Substitution - Missense |
c.209C>T; p.S70L; 20:37384362-37384362 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1554C>T; p.F518F; 20:37403322-37403322 |
skin | malignant_melanoma | Substitution - coding silent |
c.1611G>AA; p.?; 20:37403379-37403380 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Unknown |
c.1282C>T; p.P428S; 20:37402760-37402760 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.1024G>A; p.E342K; 20:37400279-37400279 |
skin | malignant_melanoma | Substitution - Missense |
c.1536C>T; p.F512F; 20:37403304-37403304 |
skin | malignant_melanoma | Substitution - coding silent |
c.525C>T; p.F175F; 20:37394249-37394249 |
skin | malignant_melanoma | Substitution - coding silent |
c.1485C>G; p.H495Q; 20:37403253-37403253 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1533C>T; p.T511T; 20:37403301-37403301 |
skin | malignant_melanoma | Substitution - coding silent |
c.435C>T; p.S145S; 20:37393979-37393979 |
skin | malignant_melanoma | Substitution - coding silent |
c.60C>T; p.P20P; 20:37384213-37384213 |
skin | malignant_melanoma | Substitution - coding silent |
c.1017C>T; p.I339I; 20:37400272-37400272 |
skin | malignant_melanoma | Substitution - coding silent |
c.1017C>T; p.I339I; 20:37400272-37400272 |
skin | malignant_melanoma | Substitution - coding silent |
c.406C>T; p.P136S; 20:37393950-37393950 |
skin | malignant_melanoma | Substitution - Missense |
c.1065G>A; p.G355G; 20:37401627-37401627 |
skin | malignant_melanoma | Substitution - coding silent |
c.1517C>T; p.P506L; 20:37403285-37403285 |
skin | malignant_melanoma | Substitution - Missense |
c.1517C>T; p.P506L; 20:37403285-37403285 |
skin | malignant_melanoma | Substitution - Missense |
c.780G>T; p.K260N; 20:37397775-37397775 |
soft_tissue; striated_muscle | rhabdomyosarcoma; embryonal | Substitution - Missense |
c.1360C>G; p.L454V; 20:37402838-37402838 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.658C>A; p.R220S; 20:37396266-37396266 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.678G>T; p.L226L; 20:37396286-37396286 |
thyroid | other; neoplasm | Substitution - coding silent |
c.1521G>C; p.E507D; 20:37403289-37403289 |
thyroid | carcinoma | Substitution - Missense |
c.1218G>C; p.A406A; 20:37402536-37402536 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.76G>A; p.G26S; 20:37384229-37384229 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.541G>A; p.E181K; 20:37394265-37394265 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1171C>T; p.R391C; 20:37402489-37402489 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.17G>A; p.S6N; 20:37384170-37384170 |
urinary_tract; bladder | carcinoma | Substitution - Missense |