Primary Site >> Stomach Cancer

Gene >> TXNRD1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000525566
Start 104321284:104321284(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1183A>T
AA Mutation p.Ile395Phe(p.I395F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000525566
Start 104289021:104289021(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.395G>A
AA Mutation p.Gly132Asp(p.G132D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000525566
Start 104311389:104311389(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.514T>C
AA Mutation p.Ser172Pro(p.S172P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000525566
Start 104348393:104348393(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1922G>A
AA Mutation p.Ser641Asn(p.S641N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000525566
Start 104288969:104288969(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.343G>T
AA Mutation p.Ala115Ser(p.A115S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000525566
Start 104339153:104339153(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1761C>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence splice_donor_variant
Transcription ID ENST00000525566
Start 104339275:104339275(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1881+2T>C
Mutation Classification Splice_Site
Feature Type Transcript