Primary Site >> Liver Cancer

Gene >> FIGN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000333129
Start 163609680:163609680(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2152C>A
AA Mutation p.Pro718Thr(p.P718T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000333129
Start 163611734:163611734(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.98G>C
AA Mutation p.Arg33Pro(p.R33P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000333129
Start 163611188:163611188(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.644A>G
AA Mutation p.His215Arg(p.H215R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000333129
Start 163611280:163611280(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.552A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000333129
Start 163610284:163610284(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1548G>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000333129
Start 163610970:163610971(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.861dupC
AA Mutation p.Thr288HisfsTer79(p.T288Hfs*79)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript