Primary Site >> Stomach Cancer

Gene >> PSG5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000342951
Start 43184830:43184830(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.382G>A
AA Mutation p.Gly128Ser(p.G128S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000342951
Start 43184992:43184992(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776252761
CDS Mutation c.220G>A
AA Mutation p.Asp74Asn(p.D74N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000342951
Start 43175914:43175914(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.665G>A
AA Mutation p.Arg222Gln(p.R222Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000342951
Start 43170135:43170135(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367783258
CDS Mutation c.968C>T
AA Mutation p.Pro323Leu(p.P323L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000342951
Start 43176090:43176090(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.489T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000342951
Start 43175937:43175937(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.642C>A
Mutation Classification Silent
Feature Type Transcript