Primary Site >> Liver Cancer

Gene >> SLC5A1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000266088
Start 32091711:32091711(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1229A>G
AA Mutation p.Tyr410Cys(p.Y410C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000266088
Start 32068566:32068566(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.443T>A
AA Mutation p.Leu148Gln(p.L148Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000266088
Start 32066995:32066995(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.268A>C
AA Mutation p.Thr90Pro(p.T90P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000266088
Start 32084998:32084998(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.984G>A
AA Mutation p.Met328Ile(p.M328I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000266088
Start 32099300:32099300(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1398C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID ENST00000266088
Start 32084434:32084450(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.665-4_677delCCAGCTTTTCACGAAGT
Mutation Classification Splice_Site
Feature Type Transcript