Primary Site >> Liver Cancer

Gene >> MCM10

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000484800
Start 13175598:13175598(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.684A>T
AA Mutation p.Arg228Ser(p.R228S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000484800
Start 13197672:13197672(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2027C>T
AA Mutation p.Thr676Ile(p.T676I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000484800
Start 13170934:13170934(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs571506868
CDS Mutation c.20A>G
AA Mutation p.Asn7Ser(p.N7S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000484800
Start 13172750:13172750(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.580A>G
AA Mutation p.Lys194Glu(p.K194E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000484800
Start 13198796:13198796(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2230A>G
AA Mutation p.Ile744Val(p.I744V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000484800
Start 13192349:13192349(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1614C>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000484800
Start 13201528:13201528(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2349C>A
AA Mutation p.Cys783Ter(p.C783*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript