Primary Site >> Stomach Cancer

Gene >> HSD17B1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000585807
Start 42553532:42553532(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.359T>G
AA Mutation p.Val120Gly(p.V120G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000585807
Start 42554482:42554482(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.617A>C
AA Mutation p.Asp206Ala(p.D206A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000585807
Start 42553589:42553589(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.416T>C
AA Mutation p.Leu139Ser(p.L139S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000585807
Start 42553196:42553196(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs61738807
CDS Mutation c.170C>T
AA Mutation p.Pro57Leu(p.P57L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000585807
Start 42553470:42553470(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.297G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000585807
Start 42553446:42553446(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.273C>T
Mutation Classification Silent
Feature Type Transcript