Primary Site >> Liver Cancer

Gene >> SYNGAP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000629380
Start 33443389:33443389(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2837G>C
AA Mutation p.Gly946Ala(p.G946A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000629380
Start 33443104:33443104(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2552C>T
AA Mutation p.Pro851Leu(p.P851L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000629380
Start 33444567:33444567(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3532T>C
AA Mutation p.Tyr1178His(p.Y1178H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000629380
Start 33437678:33437678(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs538281267
CDS Mutation c.773G>A
AA Mutation p.Arg258His(p.R258H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000629380
Start 33435259:33435259(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.617T>C
AA Mutation p.Ile206Thr(p.I206T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000629380
Start 33446667:33446667(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3675C>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000629380
Start 33437763:33437763(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.858G>T
Mutation Classification Silent
Feature Type Transcript