Primary Site >> Stomach Cancer

Gene >> PSEN2

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000366783
Start 226883918:226883918(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.355C>T
AA Mutation p.Leu119Phe(p.L119F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000366783
Start 226888966:226888966(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.704T>G
AA Mutation p.Ile235Ser(p.I235S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000366783
Start 226894036:226894036(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1102A>G
AA Mutation p.Ile368Val(p.I368V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000366783
Start 226891348:226891348(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747932826
CDS Mutation c.957C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000366783
Start 226894080:226894080(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760432548
CDS Mutation c.1146C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000366783
Start 226888844:226888844(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.582C>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence splice_donor_variant
Transcription ID ENST00000366783
Start 226888160:226888160(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.566+2T>C
Mutation Classification Splice_Site
Feature Type Transcript