Primary Site >> Liver Cancer

Gene >> SCN11A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302328
Start 38846735:38846735(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5335T>A
AA Mutation p.Ser1779Thr(p.S1779T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000302328
Start 38863250:38863250(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4001A>T
AA Mutation p.Asn1334Ile(p.N1334I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302328
Start 38903936:38903936(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1771A>T
AA Mutation p.Thr591Ser(p.T591S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000302328
Start 38950141:38950141(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.222A>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000302328
Start 38880022:38880022(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3321A>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000302328
Start 38897073:38897073(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2175T>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000302328
Start 38921233:38921233(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.735C>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000302328
Start 38885343:38885343(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3009T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000302328
Start 38910095:38910095(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1072delC
AA Mutation p.Gln358LysfsTer34(p.Q358Kfs*34)
Mutation Classification Frame_Shift_Del
Feature Type Transcript