Primary Site >> Stomach Cancer

Gene >> MPND

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262966
Start 4357409:4357409(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377098672
CDS Mutation c.1153G>A
AA Mutation p.Ala385Thr(p.A385T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262966
Start 4345896:4345896(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.446A>C
AA Mutation p.Lys149Thr(p.K149T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000262966
Start 4357375:4357375(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1119G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000262966
Start 4355008:4355008(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373394568
CDS Mutation c.906C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000262966
Start 4357348:4357348(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200486806
CDS Mutation c.1092C>T
Mutation Classification Silent
Feature Type Transcript