Primary Site >> Liver Cancer

Gene >> RUNX1T1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265814
Start 91970726:91970726(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756883632
CDS Mutation c.1471G>A
AA Mutation p.Ala491Thr(p.A491T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265814
Start 92011047:92011047(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.513A>T
AA Mutation p.Glu171Asp(p.E171D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000265814
Start 91970830:91970830(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1367T>A
AA Mutation p.Val456Glu(p.V456E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000265814
Start 91986180:91986180(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777917271
CDS Mutation c.1223G>A
AA Mutation p.Ser408Asn(p.S408N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000265814
Start 91991740:91991740(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.890C>T
AA Mutation p.Pro297Leu(p.P297L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000265814
Start 91991703:91991703(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.927C>G
AA Mutation p.His309Gln(p.H309Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000265814
Start 92014733:92014733(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.314C>T
AA Mutation p.Ser105Phe(p.S105F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000265814
Start 92014746:92014746(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.301C>T
AA Mutation p.Pro101Ser(p.P101S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000265814
Start 92011014:92011014(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.546C>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000265814
Start 92076044:92076044(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9T>A
Mutation Classification Silent
Feature Type Transcript