Primary Site >> Liver Cancer

Gene >> RALGAPA2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000202677
Start 20526350:20526350(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3595A>C
AA Mutation p.Ile1199Leu(p.I1199L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000202677
Start 20583219:20583219(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2538T>A
AA Mutation p.Ser846Arg(p.S846R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000202677
Start 20601786:20601786(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147045442
CDS Mutation c.2099G>A
AA Mutation p.Arg700Gln(p.R700Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000202677
Start 20591247:20591247(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2271G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000202677
Start 20640801:20640801(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.450G>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000202677
Start 20620601:20620601(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1263T>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000202677
Start 20605182:20605182(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2031A>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000202677
Start 20524436:20524436(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3870C>T
Mutation Classification Silent
Feature Type Transcript