Primary Site >> Stomach Cancer

Gene >> OLFM1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000371793
Start 135106847:135106847(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780417215
CDS Mutation c.775G>A
AA Mutation p.Asp259Asn(p.D259N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000371793
Start 135119960:135119960(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766525119
CDS Mutation c.1240G>A
AA Mutation p.Val414Ile(p.V414I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000371793
Start 135106854:135106854(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749666045
CDS Mutation c.782G>A
AA Mutation p.Arg261Gln(p.R261Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000371793
Start 135119598:135119598(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.878G>A
AA Mutation p.Arg293His(p.R293H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000371793
Start 135119540:135119540(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368339499
CDS Mutation c.820G>A
AA Mutation p.Val274Ile(p.V274I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000371793
Start 135090298:135090298(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.254G>A
AA Mutation p.Cys85Tyr(p.C85Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000371793
Start 135119720:135119720(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771847269
CDS Mutation c.1000C>T
AA Mutation p.Arg334Cys(p.R334C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000371793
Start 135120166:135120166(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773741461
CDS Mutation c.1446C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000371793
Start 135119512:135119512(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.792C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000371793
Start 135098492:135098492(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.663C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000371793
Start 135119524:135119524(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.804T>A
AA Mutation p.Tyr268Ter(p.Y268*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000371793
Start 135120026:135120026(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1306G>T
AA Mutation p.Glu436Ter(p.E436*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript