Primary Site >> Liver Cancer

Gene >> MORC1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000232603
Start 108979599:108979599(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2393G>T
AA Mutation p.Gly798Val(p.G798V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000232603
Start 109114405:109114405(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.98C>T
AA Mutation p.Ala33Val(p.A33V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000232603
Start 109005093:109005093(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1990G>T
AA Mutation p.Val664Phe(p.V664F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000232603
Start 108979602:108979602(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2390G>A
AA Mutation p.Ser797Asn(p.S797N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000232603
Start 109100494:109100494(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.237C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000232603
Start 109054876:109054876(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1182C>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000232603
Start 109099460:109099460(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.321C>T
Mutation Classification Silent
Feature Type Transcript