Primary Site >> Stomach Cancer

Gene >> PRKAA2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000371244
Start 56674410:56674410(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.124G>C
AA Mutation p.Val42Leu(p.V42L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000371244
Start 56704045:56704045(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.863T>C
AA Mutation p.Ile288Thr(p.I288T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000371244
Start 56704254:56704254(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1072C>T
AA Mutation p.His358Tyr(p.H358Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000371244
Start 56707555:56707555(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1501A>T
AA Mutation p.Ser501Cys(p.S501C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000371244
Start 56704354:56704354(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1172A>G
AA Mutation p.Lys391Arg(p.K391R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000371244
Start 56704270:56704270(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1088T>C
AA Mutation p.Leu363Pro(p.L363P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000371244
Start 56704143:56704143(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.961G>C
AA Mutation p.Ala321Pro(p.A321P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000371244
Start 56704263:56704263(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1081C>A
AA Mutation p.Pro361Thr(p.P361T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000371244
Start 56704007:56704007(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.825C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000371244
Start 56696103:56696103(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.732C>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000371244
Start 56692393:56692393(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.366G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000371244
Start 56693835:56693835(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.546T>C
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000371244
Start 56707668:56707668(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1620delT
AA Mutation p.Phe540LeufsTer7(p.F540Lfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000371244
Start 56704075:56704075(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.897delA
AA Mutation p.Lys299AsnfsTer9(p.K299Nfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000371244
Start 56704260:56704260(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1082delC
AA Mutation p.Pro361GlnfsTer3(p.P361Qfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript