Primary Site >> Stomach Cancer

Gene >> ASS1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000352480
Start 130479731:130479731(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.704T>C
AA Mutation p.Val235Ala(p.V235A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000352480
Start 130480425:130480425(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762387914
CDS Mutation c.814C>T
AA Mutation p.Arg272Cys(p.R272C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000352480
Start 130480405:130480405(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs398123131
CDS Mutation c.794G>A
AA Mutation p.Arg265His(p.R265H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000352480
Start 130479799:130479799(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765748014
CDS Mutation c.772G>A
AA Mutation p.Ala258Thr(p.A258T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000352480
Start 130476943:130476943(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764331417
CDS Mutation c.670G>A
AA Mutation p.Glu224Lys(p.E224K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000352480
Start 130466761:130466761(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs576636333
CDS Mutation c.457C>T
AA Mutation p.Arg153Trp(p.R153W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000352480
Start 130479749:130479749(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.722G>A
AA Mutation p.Gly241Asp(p.G241D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000352480
Start 130464121:130464121(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.374A>G
AA Mutation p.Gln125Arg(p.Q125R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000352480
Start 130479732:130479732(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.705G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000352480
Start 130454368:130454368(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.173delA
AA Mutation p.Lys58ArgfsTer82(p.K58Rfs*82)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000352480
Start 130464153:130464154(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.412dupC
AA Mutation p.Gln138ProfsTer12(p.Q138Pfs*12)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript