Primary Site >> Liver Cancer

Gene >> MED12

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000374080
Start 71120988:71120988(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.571A>T
AA Mutation p.Thr191Ser(p.T191S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000374080
Start 71134792:71134792(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4807C>A
AA Mutation p.Gln1603Lys(p.Q1603K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000374080
Start 71129424:71129424(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3686T>A
AA Mutation p.Val1229Glu(p.V1229E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000374080
Start 71127057:71127057(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2774G>T
AA Mutation p.Cys925Phe(p.C925F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000374080
Start 71118782:71118782(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.28G>C
AA Mutation p.Glu10Gln(p.E10Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000374080
Start 71132398:71132398(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4275A>G
Mutation Classification Silent
Feature Type Transcript