Primary Site >> Stomach Cancer

Gene >> SLC5A1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000266088
Start 32102194:32102194(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1622T>C
AA Mutation p.Ile541Thr(p.I541T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000266088
Start 32083104:32083104(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.614C>T
AA Mutation p.Thr205Ile(p.T205I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000266088
Start 32084556:32084556(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.782A>C
AA Mutation p.Asp261Ala(p.D261A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000266088
Start 32068599:32068599(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.476C>T
AA Mutation p.Ser159Leu(p.S159L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000266088
Start 32102067:32102067(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1495C>T
AA Mutation p.Arg499Cys(p.R499C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000266088
Start 32099197:32099197(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1295T>C
AA Mutation p.Val432Ala(p.V432A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000266088
Start 32066991:32066991(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.264C>T
Mutation Classification Silent
Feature Type Transcript