Primary Site >> Stomach Cancer

Gene >> PTPN9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000618819
Start 75490275:75490275(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.995G>A
AA Mutation p.Arg332His(p.R332H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000618819
Start 75470745:75470745(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1294A>G
AA Mutation p.Thr432Ala(p.T432A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000618819
Start 75527147:75527147(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs114183309
CDS Mutation c.178C>T
AA Mutation p.Arg60Cys(p.R60C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000618819
Start 75479908:75479908(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1069T>C
AA Mutation p.Tyr357His(p.Y357H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000618819
Start 75468913:75468913(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371391546
CDS Mutation c.1638G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000618819
Start 75505689:75505689(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.954T>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000618819
Start 75473715:75473715(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1182delA
AA Mutation p.Val395SerfsTer3(p.V395Sfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript