Primary Site >> Liver Cancer

Gene >> NCOA2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000452400
Start 70121331:70121331(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs61754973
CDS Mutation c.4354A>G
AA Mutation p.Met1452Val(p.M1452V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000452400
Start 70126888:70126888(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3841G>A
AA Mutation p.Gly1281Ser(p.G1281S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000452400
Start 70174798:70174798(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.321G>T
AA Mutation p.Gln107His(p.Q107H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000452400
Start 70156660:70156660(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1705A>G
AA Mutation p.Met569Val(p.M569V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000452400
Start 70123890:70123890(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781256206
CDS Mutation c.4287C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000452400
Start 70216713:70216713(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.33C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000452400
Start 70124843:70124843(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3939A>G
Mutation Classification Silent
Feature Type Transcript