Primary Site >> Liver Cancer

Gene >> SCN2A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000283256
Start 165388994:165388994(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5188G>T
AA Mutation p.Asp1730Tyr(p.D1730Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000283256
Start 165373225:165373225(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3850G>C
AA Mutation p.Val1284Leu(p.V1284L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000283256
Start 165354280:165354280(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3008T>C
AA Mutation p.Leu1003Pro(p.L1003P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000283256
Start 165310368:165310368(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.743T>C
AA Mutation p.Leu248Pro(p.L248P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000283256
Start 165354535:165354535(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3263A>G
AA Mutation p.Asp1088Gly(p.D1088G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000283256
Start 165389394:165389394(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5588A>T
AA Mutation p.Lys1863Met(p.K1863M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000283256
Start 165315590:165315590(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1503G>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000283256
Start 165386946:165386946(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4752T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000283256
Start 165389447:165389447(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5641delG
AA Mutation p.Glu1881SerfsTer20(p.E1881Sfs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript