Primary Site >> Liver Cancer

Gene >> STAB1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000321725
Start 52520816:52520816(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5719G>T
AA Mutation p.Ala1907Ser(p.A1907S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000321725
Start 52501645:52501645(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.223G>C
AA Mutation p.Val75Leu(p.V75L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000321725
Start 52504038:52504038(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1033A>T
AA Mutation p.Arg345Trp(p.R345W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000321725
Start 52516745:52516745(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4340C>A
AA Mutation p.Ser1447Tyr(p.S1447Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000321725
Start 52517059:52517059(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144391932
CDS Mutation c.4439G>A
AA Mutation p.Arg1480Gln(p.R1480Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000321725
Start 52513170:52513170(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3199G>T
AA Mutation p.Ala1067Ser(p.A1067S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000321725
Start 52520826:52520826(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5729G>T
AA Mutation p.Arg1910Leu(p.R1910L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000321725
Start 52515439:52515439(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3881G>T
AA Mutation p.Ser1294Ile(p.S1294I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000321725
Start 52519338:52519338(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5109C>A
AA Mutation p.Phe1703Leu(p.F1703L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000321725
Start 52519276:52519276(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5047C>T
AA Mutation p.Leu1683Phe(p.L1683F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000321725
Start 52512342:52512342(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2885C>T
AA Mutation p.Ala962Val(p.A962V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000321725
Start 52524195:52524195(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7638C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000321725
Start 52524192:52524192(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7635C>T
Mutation Classification Silent
Feature Type Transcript