Primary Site >> Liver Cancer

Gene >> FSTL5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000306100
Start 161386345:161386345(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1946C>T
AA Mutation p.Pro649Leu(p.P649L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000306100
Start 161776042:161776042(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.442A>C
AA Mutation p.Met148Leu(p.M148L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000306100
Start 162033630:162033630(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.155T>A
AA Mutation p.Val52Asp(p.V52D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000306100
Start 161500081:161500081(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771029095
CDS Mutation c.1393A>G
AA Mutation p.Ile465Val(p.I465V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000306100
Start 161385995:161385995(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2296G>A
AA Mutation p.Val766Met(p.V766M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000306100
Start 161759492:161759492(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.646T>C
AA Mutation p.Cys216Arg(p.C216R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000306100
Start 161386050:161386050(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2241C>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000306100
Start 161656361:161656361(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.861T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000306100
Start 161510401:161510401(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1336G>T
AA Mutation p.Glu446Ter(p.E446*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript