Primary Site >> Stomach Cancer

Gene >> PREP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369110
Start 105278350:105278350(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772490679
CDS Mutation c.1927C>T
AA Mutation p.Arg643Cys(p.R643C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369110
Start 105368968:105368968(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145682559
CDS Mutation c.652G>A
AA Mutation p.Asp218Asn(p.D218N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000369110
Start 105377387:105377387(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.253C>T
AA Mutation p.Arg85Trp(p.R85W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000369110
Start 105323757:105323757(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1225C>A
AA Mutation p.His409Asn(p.H409N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000369110
Start 105333436:105333436(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs535207006
CDS Mutation c.893C>T
AA Mutation p.Thr298Met(p.T298M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000369110
Start 105282570:105282570(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1562C>T
AA Mutation p.Ala521Val(p.A521V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000369110
Start 105288796:105288796(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1416C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000369110
Start 105333480:105333480(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.849T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000369110
Start 105288871:105288871(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1341T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000369110
Start 105278269:105278269(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2008delC
AA Mutation p.Leu670CysfsTer20(p.L670Cfs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000369110
Start 105288838:105288838(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1374delA
AA Mutation p.Gly459AlafsTer2(p.G459Afs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript