Primary Site >> Stomach Cancer

Gene >> BPHL

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000380379
Start 3152529:3152529(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs151267393
CDS Mutation c.830G>A
AA Mutation p.Arg277His(p.R277H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000380379
Start 3137444:3137444(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.615C>A
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000380379
Start 3140441:3140441(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs553521784
CDS Mutation c.720C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000380379
Start 3127351:3127351(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771151708
CDS Mutation c.321C>T
Mutation Classification Silent
Feature Type Transcript