Primary Site >> Liver Cancer

Gene >> TIAM2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000318981
Start 155183272:155183272(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2836G>T
AA Mutation p.Gly946Trp(p.G946W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000318981
Start 155176936:155176936(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2482C>T
AA Mutation p.Pro828Ser(p.P828S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000318981
Start 155176882:155176882(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2428A>T
AA Mutation p.Ile810Phe(p.I810F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000318981
Start 155129830:155129830(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.607A>C
AA Mutation p.Thr203Pro(p.T203P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000318981
Start 155137420:155137420(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1438A>T
AA Mutation p.Thr480Ser(p.T480S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000318981
Start 155137213:155137213(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1231A>T
AA Mutation p.Ser411Cys(p.S411C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000318981
Start 155248046:155248046(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3699C>T
Mutation Classification Silent
Feature Type Transcript