Primary Site >> Liver Cancer

Gene >> BCL11B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000357195
Start 99175374:99175374(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1462T>A
AA Mutation p.Ser488Thr(p.S488T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000357195
Start 99176012:99176012(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.824C>T
AA Mutation p.Ala275Val(p.A275V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000357195
Start 99174630:99174630(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2206C>A
AA Mutation p.Pro736Thr(p.P736T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000357195
Start 99174594:99174594(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2242G>A
AA Mutation p.Gly748Ser(p.G748S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000357195
Start 99174376:99174376(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2460C>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000357195
Start 99175326:99175326(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1510G>T
AA Mutation p.Glu504Ter(p.E504*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000357195
Start 99175471:99175471(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1365C>G
AA Mutation p.Tyr455Ter(p.Y455*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript