Primary Site >> Liver Cancer

Gene >> BMPER

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000297161
Start 34058083:34058083(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.952A>T
AA Mutation p.Asn318Tyr(p.N318Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000297161
Start 33937331:33937331(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.262T>C
AA Mutation p.Ser88Pro(p.S88P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000297161
Start 34153095:34153095(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143727756
CDS Mutation c.1880C>T
AA Mutation p.Thr627Ile(p.T627I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000297161
Start 34062024:34062024(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1055G>T
AA Mutation p.Gly352Val(p.G352V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000297161
Start 33974719:33974719(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.511G>A
AA Mutation p.Val171Met(p.V171M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000297161
Start 33905660:33905660(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.47G>T
AA Mutation p.Arg16Leu(p.R16L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000297161
Start 34078975:34078975(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1197G>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000297161
Start 34079131:34079131(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1353G>A
Mutation Classification Silent
Feature Type Transcript