Primary Site >> Stomach Cancer

Gene >> NR1I3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000367982
Start 161231239:161231239(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.701C>A
AA Mutation p.Pro234His(p.P234H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000367982
Start 161233327:161233327(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.250G>A
AA Mutation p.Ala84Thr(p.A84T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000367982
Start 161233247:161233247(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.330A>C
AA Mutation p.Gln110His(p.Q110H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000367982
Start 161229866:161229866(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs79799851
CDS Mutation c.990C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000367982
Start 161231408:161231408(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.615A>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000367982
Start 161233280:161233280(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.297A>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000367982
Start 161232892:161232892(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.463C>T
Mutation Classification Silent
Feature Type Transcript