Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PRPF6

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000266079
Start 63983048:63983048(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.73G>A
AA Mutation p.Ala25Thr(p.A25T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 64010299:64010299(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1286G>A
AA Mutation p.Cys429Tyr(p.C429Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 64011454:64011454(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1475C>T
AA Mutation p.Thr492Ile(p.T492I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 64027684:64027684(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2287C>T
AA Mutation p.Arg763Trp(p.R763W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 63999640:63999640(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.904C>T
AA Mutation p.Arg302Trp(p.R302W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 64022845:64022845(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1736G>A
AA Mutation p.Arg579His(p.R579H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 63983067:63983067(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.92G>A
AA Mutation p.Arg31Gln(p.R31Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 64016837:64016837(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1639G>A
AA Mutation p.Ala547Thr(p.A547T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 63999617:63999617(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.881C>T
AA Mutation p.Ala294Val(p.A294V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 64024624:64024624(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1839G>T
AA Mutation p.Met613Ile(p.M613I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 63999656:63999656(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.920A>T
AA Mutation p.His307Leu(p.H307L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 63983066:63983066(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.91C>T
AA Mutation p.Arg31Trp(p.R31W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 64027722:64027722(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2325G>T
AA Mutation p.Lys775Asn(p.K775N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 63983114:63983114(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.139C>T
AA Mutation p.Arg47Cys(p.R47C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 64027726:64027726(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2329C>A
AA Mutation p.Pro777Thr(p.P777T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 63999685:63999685(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.949C>T
AA Mutation p.Arg317Cys(p.R317C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 64010205:64010205(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1192G>A
AA Mutation p.Glu398Lys(p.E398K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000266079
Start 64032927:64032927(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2760C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000266079
Start 64027047:64027047(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767213788
CDS Mutation c.2094C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 20
Mutation Consequence stop_gained
Transcription ID ENST00000266079
Start 63999619:63999619(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.883C>T
AA Mutation p.Arg295Ter(p.R295*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> PRPF6

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000266079
Start 63983048:63983048(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.73G>A
AA Mutation p.Ala25Thr(p.A25T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000266079
Start 63999732:63999732(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.996C>A
Mutation Classification Silent
Feature Type Transcript