Primary Site >> Stomach Cancer

Gene >> AP5M1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261558
Start 57274647:57274647(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.478C>T
AA Mutation p.Pro160Ser(p.P160S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261558
Start 57274722:57274722(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.553A>G
AA Mutation p.Asn185Asp(p.N185D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261558
Start 57274462:57274462(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745558945
CDS Mutation c.293C>G
AA Mutation p.Ala98Gly(p.A98G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000261558
Start 57274352:57274352(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.183A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000261558
Start 57274310:57274310(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.141A>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000261558
Start 57280290:57280290(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.816A>G
Mutation Classification Silent
Feature Type Transcript