Primary Site >> Liver Cancer

Gene >> AGAP2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000547588
Start 57727995:57727995(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2708A>T
AA Mutation p.Gln903Leu(p.Q903L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000547588
Start 57734093:57734093(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1482T>A
AA Mutation p.His494Gln(p.H494Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000547588
Start 57731926:57731926(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750480607
CDS Mutation c.1836C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000547588
Start 57727395:57727395(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3045G>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000547588
Start 57726983:57726983(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3327G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000547588
Start 57737242:57737242(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1005C>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000547588
Start 57737878:57737878(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.369C>A
Mutation Classification Silent
Feature Type Transcript