Primary Site >> Liver Cancer

Gene >> MGLL

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000398104
Start 127722467:127722467(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765489619
CDS Mutation c.332A>G
AA Mutation p.Tyr111Cys(p.Y111C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000398104
Start 127821748:127821748(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.71A>C
AA Mutation p.Asn24Thr(p.N24T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000398104
Start 127722448:127722448(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.351C>G
AA Mutation p.Phe117Leu(p.F117L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000398104
Start 127722554:127722554(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.245A>G
AA Mutation p.Gln82Arg(p.Q82R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000398104
Start 127695146:127695146(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.615G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000398104
Start 127821762:127821762(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.57C>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000398104
Start 127695185:127695185(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.576C>T
Mutation Classification Silent
Feature Type Transcript