Primary Site >> Liver Cancer

Gene >> NSD1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000439151
Start 177135318:177135318(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.215T>G
AA Mutation p.Leu72Arg(p.L72R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000439151
Start 177295370:177295370(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8002G>A
AA Mutation p.Gly2668Arg(p.G2668R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000439151
Start 177210953:177210953(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2554A>G
AA Mutation p.Ile852Val(p.I852V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000439151
Start 177294806:177294806(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7438G>A
AA Mutation p.Asp2480Asn(p.D2480N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000439151
Start 177295235:177295235(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7867A>C
AA Mutation p.Ser2623Arg(p.S2623R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000439151
Start 177135394:177135394(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.291T>G
AA Mutation p.Phe97Leu(p.F97L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000439151
Start 177294058:177294058(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6690A>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000439151
Start 177135163:177135163(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.60G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000439151
Start 177294087:177294087(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6719C>A
AA Mutation p.Ser2240Ter(p.S2240*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript