Primary Site >> Liver Cancer

Gene >> DIDO1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000266070
Start 62880360:62880360(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5596G>A
AA Mutation p.Ala1866Thr(p.A1866T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000266070
Start 62881425:62881425(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4531A>G
AA Mutation p.Met1511Val(p.M1511V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000266070
Start 62893794:62893794(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2973G>A
AA Mutation p.Met991Ile(p.M991I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000266070
Start 62891076:62891076(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3425G>A
AA Mutation p.Ser1142Asn(p.S1142N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000266070
Start 62896930:62896930(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1655C>T
AA Mutation p.Pro552Leu(p.P552L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000266070
Start 62879513:62879513(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762714731
CDS Mutation c.6443A>G
AA Mutation p.Asp2148Gly(p.D2148G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000266070
Start 62895088:62895088(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2292T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000266070
Start 62881552:62881552(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776072192
CDS Mutation c.4404G>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000266070
Start 62911097:62911097(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.516G>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000266070
Start 62906073:62906073(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1402A>T
AA Mutation p.Lys468Ter(p.K468*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000266070
Start 62894196:62894196(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2573-2A>T
Mutation Classification Splice_Site
Feature Type Transcript