Primary Site >> Stomach Cancer

Gene >> CSK

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000220003
Start 74798700:74798700(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.101A>G
AA Mutation p.Asp34Gly(p.D34G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000220003
Start 74798862:74798862(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144688425
CDS Mutation c.166C>T
AA Mutation p.Arg56Cys(p.R56C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000220003
Start 74800918:74800918(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.718A>G
AA Mutation p.Met240Val(p.M240V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000220003
Start 74801070:74801070(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754759286
CDS Mutation c.781G>A
AA Mutation p.Gly261Arg(p.G261R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000220003
Start 74802335:74802335(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1175T>C
AA Mutation p.Leu392Pro(p.L392P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000220003
Start 74799415:74799415(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.386A>G
AA Mutation p.Tyr129Cys(p.Y129C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000220003
Start 74802438:74802438(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs576918025
CDS Mutation c.1278C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000220003
Start 74798632:74798632(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.33T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000220003
Start 74798675:74798675(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.76C>T
AA Mutation p.Gln26Ter(p.Q26*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000220003
Start 74802469:74802469(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1309C>T
AA Mutation p.Arg437Ter(p.R437*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence inframe_deletion
Transcription ID ENST00000220003
Start 74802050:74802052(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1139_1141delACT
AA Mutation p.Tyr380del(p.Y380del)
Mutation Classification In_Frame_Del
Feature Type Transcript