Primary Site >> Liver Cancer

Gene >> HGF

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000222390
Start 81743459:81743459(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.759G>T
AA Mutation p.Lys253Asn(p.K253N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000222390
Start 81745082:81745082(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.664C>A
AA Mutation p.Leu222Ile(p.L222I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000222390
Start 81702714:81702714(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2054G>T
AA Mutation p.Arg685Ile(p.R685I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000222390
Start 81706382:81706382(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1662C>A
AA Mutation p.His554Gln(p.H554Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000222390
Start 81710240:81710240(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1448C>A
AA Mutation p.Pro483His(p.P483H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000222390
Start 81743428:81743428(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.790G>T
AA Mutation p.Asp264Tyr(p.D264Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000222390
Start 81725966:81725966(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1092G>C
AA Mutation p.Trp364Cys(p.W364C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000222390
Start 81702659:81702659(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2109T>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000222390
Start 81710239:81710239(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1449C>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID ENST00000222390
Start 81720845:81720881(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1169-34_1171delTCATTGGACTTATTTCTGTATATTTTATGTCTAGATT
Mutation Classification Splice_Site
Feature Type Transcript