Primary Site >> Liver Cancer

Gene >> NUP153

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262077
Start 17675567:17675567(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.538A>C
AA Mutation p.Asn180His(p.N180H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262077
Start 17639969:17639969(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1816G>C
AA Mutation p.Gly606Arg(p.G606R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262077
Start 17706357:17706357(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.31G>T
AA Mutation p.Gly11Cys(p.G11C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262077
Start 17637444:17637444(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2173A>G
AA Mutation p.Thr725Ala(p.T725A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000262077
Start 17628768:17628768(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3431A>G
AA Mutation p.Glu1144Gly(p.E1144G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000262077
Start 17616571:17616571(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4299G>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000262077
Start 17629232:17629232(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2967A>G
Mutation Classification Silent
Feature Type Transcript