Primary Site >> Stomach Cancer

Gene >> GATA6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000269216
Start 22171487:22171487(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.343T>C
AA Mutation p.Phe115Leu(p.F115L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000269216
Start 22182835:22182835(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1507A>T
AA Mutation p.Thr503Ser(p.T503S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000269216
Start 22171573:22171573(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.429G>T
AA Mutation p.Gln143His(p.Q143H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000269216
Start 22182788:22182788(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1460G>T
AA Mutation p.Gly487Val(p.G487V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000269216
Start 22171636:22171636(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.492C>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000269216
Start 22181545:22181545(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1395C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000269216
Start 22182768:22182768(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1440A>G
Mutation Classification Silent
Feature Type Transcript