Primary Site >> Liver Cancer

Gene >> TCF4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000356073
Start 55461100:55461100(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs567398278
CDS Mutation c.223A>G
AA Mutation p.Thr75Ala(p.T75A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000356073
Start 55234683:55234683(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1351G>A
AA Mutation p.Val451Met(p.V451M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000356073
Start 55259958:55259958(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1060T>C
AA Mutation p.Ser354Pro(p.S354P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000398339
Start 55635821:55635821(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.77A>T
AA Mutation p.Tyr26Phe(p.Y26F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000356073
Start 55228303:55228303(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1926C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000356073
Start 55350959:55350959(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.414C>T
Mutation Classification Silent
Feature Type Transcript