Primary Site >> Stomach Cancer

Gene >> SLC22A7

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000372585
Start 43300002:43300002(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199806887
CDS Mutation c.763C>T
AA Mutation p.Arg255Trp(p.R255W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000372585
Start 43302352:43302352(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1214C>T
AA Mutation p.Thr405Met(p.T405M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000372585
Start 43304073:43304073(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774294045
CDS Mutation c.1421G>A
AA Mutation p.Arg474Gln(p.R474Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000372585
Start 43304142:43304142(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1490C>G
AA Mutation p.Thr497Ser(p.T497S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000372585
Start 43301655:43301655(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1024C>G
AA Mutation p.Arg342Gly(p.R342G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000372585
Start 43304147:43304147(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1495G>A
AA Mutation p.Gly499Arg(p.G499R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000372585
Start 43299449:43299449(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.459C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000372585
Start 43299437:43299437(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.447T>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000372585
Start 43304077:43304077(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1430delG
AA Mutation p.Gly477AlafsTer67(p.G477Afs*67)
Mutation Classification Frame_Shift_Del
Feature Type Transcript