Primary Site >> Pancreatic Cancer

Gene >> GRM1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000282753
Start 146159561:146159561(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.914G>A
AA Mutation p.Arg305His(p.R305H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000282753
Start 146434284:146434284(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3073C>G
AA Mutation p.Pro1025Ala(p.P1025A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000282753
Start 146029645:146029645(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.128G>T
AA Mutation p.Gly43Val(p.G43V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000282753
Start 146304669:146304669(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1009G>A
AA Mutation p.Gly337Arg(p.G337R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000282753
Start 146029857:146029857(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.340G>A
AA Mutation p.Val114Met(p.V114M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000282753
Start 146030051:146030051(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.534C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000282753
Start 146357571:146357571(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1479C>T
Mutation Classification Silent
Feature Type Transcript