Primary Site >> Liver Cancer

Gene >> RTN4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000337526
Start 55025178:55025178(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2921T>C
AA Mutation p.Val974Ala(p.V974A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000337526
Start 55027045:55027045(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1054A>G
AA Mutation p.Lys352Glu(p.K352E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000337526
Start 54974739:54974739(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3386C>T
AA Mutation p.Thr1129Ile(p.T1129I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000337526
Start 55027480:55027480(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.619A>G
AA Mutation p.Met207Val(p.M207V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000337526
Start 55027482:55027482(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.617A>C
AA Mutation p.Asn206Thr(p.N206T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000337526
Start 55025972:55025972(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2127T>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000337526
Start 55026740:55026740(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1359T>C
Mutation Classification Silent
Feature Type Transcript