Primary Site >> Stomach Cancer

Gene >> PTPN22

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359785
Start 113838066:113838066(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1334C>G
AA Mutation p.Thr445Arg(p.T445R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359785
Start 113838063:113838063(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs267597928
CDS Mutation c.1337G>A
AA Mutation p.Arg446Gln(p.R446Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359785
Start 113838075:113838075(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1325T>C
AA Mutation p.Val442Ala(p.V442A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359785
Start 113838070:113838070(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1330A>G
AA Mutation p.Ile444Val(p.I444V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359785
Start 113814922:113814922(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2407C>T
AA Mutation p.Pro803Ser(p.P803S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000359785
Start 113834987:113834987(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1817C>A
AA Mutation p.Ala606Asp(p.A606D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000359785
Start 113859038:113859038(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.237T>C
Mutation Classification Silent
Feature Type Transcript