Primary Site >> Stomach Cancer

Gene >> PHOSPHO2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359744
Start 169701560:169701560(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.589A>T
AA Mutation p.Met197Leu(p.M197L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359744
Start 169701521:169701521(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.550G>A
AA Mutation p.Val184Ile(p.V184I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359744
Start 169700994:169700994(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.23A>G
AA Mutation p.Asp8Gly(p.D8G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359744
Start 169701405:169701405(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.434A>G
AA Mutation p.Asn145Ser(p.N145S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359744
Start 169701641:169701641(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751867437
CDS Mutation c.670G>T
AA Mutation p.Val224Phe(p.V224F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000359744
Start 169701085:169701085(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.114T>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000359744
Start 169701652:169701652(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.681A>G
Mutation Classification Silent
Feature Type Transcript