Primary Site >> Liver Cancer

Gene >> NFATC2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000396009
Start 51432157:51432157(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2632G>A
AA Mutation p.Gly878Arg(p.G878R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000396009
Start 51475519:51475519(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1474A>C
AA Mutation p.Ile492Leu(p.I492L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000396009
Start 51523171:51523171(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1070A>C
AA Mutation p.Gln357Pro(p.Q357P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000396009
Start 51523367:51523367(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.874G>T
AA Mutation p.Ala292Ser(p.A292S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000396009
Start 51523655:51523655(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.586G>A
AA Mutation p.Gly196Ser(p.G196S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000396009
Start 51454637:51454637(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1760G>A
AA Mutation p.Ser587Asn(p.S587N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000396009
Start 51542437:51542437(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.63G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000396009
Start 51432123:51432138(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2651_2666delAAAAGGAAGTATTACC
AA Mutation p.Gln884LeufsTer4(p.Q884Lfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript