Primary Site >> Stomach Cancer

Gene >> ISX

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000308700
Start 35082527:35082527(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.239A>C
AA Mutation p.Lys80Thr(p.K80T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000308700
Start 35067158:35067158(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.71C>A
AA Mutation p.Pro24Gln(p.P24Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000308700
Start 35085601:35085601(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.646G>T
AA Mutation p.Gly216Cys(p.G216C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000308700
Start 35067159:35067159(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147323979
CDS Mutation c.72G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000308700
Start 35085621:35085621(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.666T>G
Mutation Classification Silent
Feature Type Transcript