Primary Site >> Stomach Cancer

Gene >> DHRS9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000357546
Start 169083399:169083399(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.384G>T
AA Mutation p.Glu128Asp(p.E128D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000357546
Start 169083515:169083515(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.500G>A
AA Mutation p.Gly167Asp(p.G167D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000357546
Start 169095618:169095618(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.811G>A
AA Mutation p.Ala271Thr(p.A271T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000357546
Start 169081814:169081814(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.233G>A
AA Mutation p.Arg78His(p.R78H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000357546
Start 169081785:169081785(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.204T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000357546
Start 169083345:169083345(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.330C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000357546
Start 169095659:169095659(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.855delA
AA Mutation p.Asp286MetfsTer22(p.D286Mfs*22)
Mutation Classification Frame_Shift_Del
Feature Type Transcript