Primary Site >> Stomach Cancer

Gene >> PRND

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000305817
Start 4725018:4725018(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773175272
CDS Mutation c.467G>A
AA Mutation p.Arg156Gln(p.R156Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000305817
Start 4724660:4724660(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748124038
CDS Mutation c.109C>T
AA Mutation p.Arg37Trp(p.R37W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000305817
Start 4725065:4725065(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.514T>C
AA Mutation p.Trp172Arg(p.W172R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000305817
Start 4724884:4724884(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.333C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000305817
Start 4724749:4724749(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369768460
CDS Mutation c.198C>T
Mutation Classification Silent
Feature Type Transcript