Primary Site >> Liver Cancer

Gene >> NXF3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000395065
Start 103082821:103082821(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.719C>A
AA Mutation p.Ala240Glu(p.A240E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000395065
Start 103079360:103079360(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761308991
CDS Mutation c.1334C>T
AA Mutation p.Thr445Met(p.T445M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000395065
Start 103083496:103083496(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.442T>A
AA Mutation p.Tyr148Asn(p.Y148N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000395065
Start 103079236:103079236(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751182875
CDS Mutation c.1363G>A
AA Mutation p.Gly455Arg(p.G455R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000395065
Start 103080166:103080166(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.978G>T
AA Mutation p.Lys326Asn(p.K326N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000395065
Start 103077692:103077692(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1506C>G
Mutation Classification Silent
Feature Type Transcript