Primary Site >> Liver Cancer

Gene >> GRM1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000282753
Start 146399578:146399578(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2539C>G
AA Mutation p.Arg847Gly(p.R847G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000282753
Start 146434599:146434599(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3388G>T
AA Mutation p.Asp1130Tyr(p.D1130Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000282753
Start 146434189:146434189(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2978C>T
AA Mutation p.Ser993Phe(p.S993F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000282753
Start 146434380:146434380(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3169G>T
AA Mutation p.Gly1057Cys(p.G1057C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000282753
Start 146159517:146159517(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.870C>A
AA Mutation p.Phe290Leu(p.F290L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000282753
Start 146386930:146386930(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1643C>A
AA Mutation p.Thr548Lys(p.T548K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000282753
Start 146434455:146434455(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3244C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000282753
Start 146399172:146399172(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2133A>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000282753
Start 146159400:146159400(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.753A>G
Mutation Classification Silent
Feature Type Transcript