Primary Site >> Liver Cancer

Gene >> NRXN1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000406316
Start 50091335:50091335(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3706C>T
AA Mutation p.Arg1236Cys(p.R1236C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000406316
Start 50538361:50538361(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2035C>A
AA Mutation p.Pro679Thr(p.P679T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000406316
Start 50236794:50236794(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377333818
CDS Mutation c.3541C>A
AA Mutation p.His1181Asn(p.H1181N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000406316
Start 50053329:50053329(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3980C>G
AA Mutation p.Thr1327Ser(p.T1327S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000406316
Start 51027685:51027685(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369183287
CDS Mutation c.589G>A
AA Mutation p.Val197Met(p.V197M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000406316
Start 51027867:51027867(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202118977
CDS Mutation c.407A>G
AA Mutation p.Lys136Arg(p.K136R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000406316
Start 50531250:50531250(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369744946
CDS Mutation c.2324G>A
AA Mutation p.Arg775His(p.R775H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000406316
Start 50236879:50236879(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3456G>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000406316
Start 50236837:50236837(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3498G>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000406316
Start 50472329:50472329(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3213C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000406316
Start 50236836:50236836(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3499C>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000406316
Start 51027614:51027614(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.660C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000406316
Start 51028195:51028195(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.79C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000406316
Start 51028229:51028229(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.45C>A
AA Mutation p.Cys15Ter(p.C15*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000406316
Start 49922083:49922083(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4295C>A
AA Mutation p.Ser1432Ter(p.S1432*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript