Primary Site >> Liver Cancer

Gene >> NALCN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000251127
Start 101103192:101103192(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773376286
CDS Mutation c.3037G>A
AA Mutation p.Gly1013Ser(p.G1013S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000251127
Start 101065461:101065461(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4547G>A
AA Mutation p.Cys1516Tyr(p.C1516Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000251127
Start 101074587:101074587(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4030C>G
AA Mutation p.Leu1344Val(p.L1344V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000251127
Start 101107590:101107590(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2476C>A
AA Mutation p.Leu826Ile(p.L826I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000251127
Start 101082848:101082848(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3726A>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence inframe_deletion
Transcription ID ENST00000251127
Start 101068738:101068782(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4243_4287delACAGACTGTGGAAATTATGCTGGGGCACTTATGTATTTCTGTTCA
AA Mutation p.Thr1415_Ser1429del(p.T1415_S1429del)
Mutation Classification In_Frame_Del
Feature Type Transcript