Primary Site >> Stomach Cancer

Gene >> HSD11B2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000326152
Start 67436292:67436292(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.708A>C
AA Mutation p.Lys236Asn(p.K236N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000326152
Start 67436719:67436719(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs564896195
CDS Mutation c.934C>T
AA Mutation p.Arg312Cys(p.R312C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000326152
Start 67436864:67436864(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1079G>A
AA Mutation p.Arg360His(p.R360H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000326152
Start 67436844:67436844(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1059C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000326152
Start 67436094:67436094(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.616C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000326152
Start 67436342:67436342(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.763delG
AA Mutation p.Val255SerfsTer16(p.V255Sfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript