Primary Site >> Stomach Cancer

Gene >> NR1H4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000551379
Start 100510967:100510967(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs113431969
CDS Mutation c.299G>A
AA Mutation p.Arg100His(p.R100H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000551379
Start 100563311:100563311(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1283T>C
AA Mutation p.Val428Ala(p.V428A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000551379
Start 100510955:100510955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.287A>T
AA Mutation p.Tyr96Phe(p.Y96F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000551379
Start 100537028:100537028(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.942A>C
AA Mutation p.Glu314Asp(p.E314D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000551379
Start 100563480:100563480(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778715261
CDS Mutation c.1452C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000551379
Start 100534945:100534945(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778260507
CDS Mutation c.684G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000551379
Start 100511046:100511046(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767379406
CDS Mutation c.378G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000551379
Start 100503432:100503432(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.45T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000551379
Start 100563317:100563317(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1292delA
AA Mutation p.Lys431SerfsTer21(p.K431Sfs*21)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence splice_donor_variant
Transcription ID ENST00000551379
Start 100537049:100537049(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.961+2T>C
Mutation Classification Splice_Site
Feature Type Transcript