Primary Site >> Stomach Cancer

Gene >> UMOD

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302509
Start 20341293:20341293(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139607138
CDS Mutation c.1375C>T
AA Mutation p.Arg459Trp(p.R459W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000302509
Start 20346127:20346127(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs532447307
CDS Mutation c.1181C>T
AA Mutation p.Thr394Met(p.T394M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302509
Start 20348522:20348522(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.779C>T
AA Mutation p.Ala260Val(p.A260V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000302509
Start 20346239:20346239(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1069G>A
AA Mutation p.Val357Ile(p.V357I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000302509
Start 20337405:20337405(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1626G>C
AA Mutation p.Glu542Asp(p.E542D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000302509
Start 20336667:20336667(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1801T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000302509
Start 20348965:20348965(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.336C>T
Mutation Classification Silent
Feature Type Transcript