Primary Site >> Stomach Cancer

Gene >> HSD17B7

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000254521
Start 162796674:162796674(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.329C>T
AA Mutation p.Ser110Leu(p.S110L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000254521
Start 162796587:162796587(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.242T>G
AA Mutation p.Phe81Cys(p.F81C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000254521
Start 162799890:162799890(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.595G>A
AA Mutation p.Ala199Thr(p.A199T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000254521
Start 162812350:162812350(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.956T>C
AA Mutation p.Leu319Pro(p.L319P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000254521
Start 162803468:162803468(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.680T>C
AA Mutation p.Leu227Ser(p.L227S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000254521
Start 162792824:162792824(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.201G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000254521
Start 162799751:162799751(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.456A>G
Mutation Classification Silent
Feature Type Transcript