Primary Site >> Stomach Cancer

Gene >> VDR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000229022
Start 47857605:47857605(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752590757
CDS Mutation c.361C>T
AA Mutation p.Arg121Trp(p.R121W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000229022
Start 47846764:47846764(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.800C>T
AA Mutation p.Ala267Val(p.A267V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000229022
Start 47844791:47844791(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1239G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000229022
Start 47879086:47879086(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.28C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence splice_donor_variant
Transcription ID ENST00000229022
Start 47878966:47878966(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.146+2T>C
Mutation Classification Splice_Site
Feature Type Transcript