Primary Site >> Liver Cancer

Gene >> TIMELESS

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000553532
Start 56418183:56418183(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3405G>T
AA Mutation p.Arg1135Ser(p.R1135S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000553532
Start 56428926:56428926(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1261A>T
AA Mutation p.Met421Leu(p.M421L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000553532
Start 56420592:56420592(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3205G>C
AA Mutation p.Val1069Leu(p.V1069L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000553532
Start 56418229:56418229(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3359G>A
AA Mutation p.Gly1120Asp(p.G1120D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000553532
Start 56420607:56420607(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs267603583
CDS Mutation c.3190T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000553532
Start 56434105:56434105(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.66A>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000553532
Start 56423664:56423664(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2010G>A
Mutation Classification Silent
Feature Type Transcript