Primary Site >> Liver Cancer

Gene >> TRPM1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000397795
Start 31030988:31030988(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3056T>C
AA Mutation p.Ile1019Thr(p.I1019T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000397795
Start 31002515:31002515(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4119A>T
AA Mutation p.Lys1373Asn(p.K1373N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000397795
Start 31032858:31032858(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2717C>T
AA Mutation p.Ala906Val(p.A906V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000397795
Start 31042161:31042161(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1811C>T
AA Mutation p.Ala604Val(p.A604V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000397795
Start 31032874:31032874(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2701A>T
AA Mutation p.Ile901Phe(p.I901F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000397795
Start 31038143:31038143(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2274C>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000397795
Start 31002860:31002860(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3774T>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000397795
Start 31001888:31001888(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4746G>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000397795
Start 31063168:31063168(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.849A>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000397795
Start 31037798:31037798(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2418C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000397795
Start 31068087:31068087(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.219C>T
Mutation Classification Silent
Feature Type Transcript