Primary Site >> Stomach Cancer

Gene >> TRAF7

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000326181
Start 2173953:2173953(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1168G>A
AA Mutation p.Gly390Arg(p.G390R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000326181
Start 2168082:2168082(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745522760
CDS Mutation c.145G>A
AA Mutation p.Gly49Arg(p.G49R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000326181
Start 2175602:2175602(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1606G>A
AA Mutation p.Gly536Ser(p.G536S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000326181
Start 2173816:2173816(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1115T>C
AA Mutation p.Leu372Pro(p.L372P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000326181
Start 2176307:2176307(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1921C>T
AA Mutation p.Arg641Cys(p.R641C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000326181
Start 2172326:2172326(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.611A>C
AA Mutation p.Glu204Ala(p.E204A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000326181
Start 2173540:2173540(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1072G>A
AA Mutation p.Ala358Thr(p.A358T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000326181
Start 2172241:2172241(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.526G>A
AA Mutation p.Ala176Thr(p.A176T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000326181
Start 2173995:2173995(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200505184
CDS Mutation c.1210G>A
AA Mutation p.Val404Ile(p.V404I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000326181
Start 2173233:2173233(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.846C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000326181
Start 2176123:2176123(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1821C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000326181
Start 2176330:2176330(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371337922
CDS Mutation c.1944G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000326181
Start 2165905:2165905(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs185257232
CDS Mutation c.108C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000326181
Start 2175923:2175926(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1719_1722delCTGT
AA Mutation p.Cys574AlafsTer59(p.C574Afs*59)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000326181
Start 2175872:2175885(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1669_1682delACGTCTGGTGGCAG
AA Mutation p.Thr557ArgfsTer26(p.T557Rfs*26)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000326181
Start 2172337:2172337(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.622C>T
AA Mutation p.Arg208Ter(p.R208*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript