Primary Site >> Stomach Cancer

Gene >> SAG

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000409110
Start 233331693:233331693(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs534274448
CDS Mutation c.787G>A
AA Mutation p.Val263Met(p.V263M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000409110
Start 233309263:233309263(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374930316
CDS Mutation c.74C>T
AA Mutation p.Ser25Leu(p.S25L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000409110
Start 233338701:233338701(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775968495
CDS Mutation c.970G>A
AA Mutation p.Val324Ile(p.V324I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000409110
Start 233331684:233331684(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.778G>A
AA Mutation p.Val260Ile(p.V260I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000409110
Start 233318759:233318759(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs151281271
CDS Mutation c.145G>A
AA Mutation p.Val49Met(p.V49M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000409110
Start 233334986:233334986(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.831T>G
Mutation Classification Silent
Feature Type Transcript