Primary Site >> Stomach Cancer

Gene >> TSG101

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000251968
Start 18480560:18480560(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1159A>G
AA Mutation p.Ser387Gly(p.S387G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000251968
Start 18483923:18483923(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.790A>G
AA Mutation p.Lys264Glu(p.K264E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000251968
Start 18509592:18509592(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376545696
CDS Mutation c.431G>A
AA Mutation p.Arg144His(p.R144H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000251968
Start 18509583:18509583(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140156278
CDS Mutation c.440C>T
AA Mutation p.Ser147Leu(p.S147L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000251968
Start 18514824:18514824(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.211C>T
AA Mutation p.Pro71Ser(p.P71S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000251968
Start 18481767:18481767(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.946G>C
AA Mutation p.Glu316Gln(p.E316Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000251968
Start 18509585:18509585(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.438T>A
Mutation Classification Silent
Feature Type Transcript