Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DAAM2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39896925:39896925(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2455G>A
AA Mutation p.Gly819Arg(p.G819R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39896910:39896910(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146966805
CDS Mutation c.2440C>T
AA Mutation p.Arg814Cys(p.R814C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39891417:39891417(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767650659
CDS Mutation c.2222G>A
AA Mutation p.Arg741His(p.R741H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39867652:39867652(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.571C>T
AA Mutation p.Arg191Trp(p.R191W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39873280:39873280(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1087A>T
AA Mutation p.Ile363Phe(p.I363F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39878425:39878425(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752703893
CDS Mutation c.1382G>A
AA Mutation p.Arg461His(p.R461H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39867680:39867680(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.599C>T
AA Mutation p.Ala200Val(p.A200V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39878583:39878583(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1540C>A
AA Mutation p.Leu514Ile(p.L514I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39871531:39871531(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371806282
CDS Mutation c.1003C>T
AA Mutation p.Arg335Trp(p.R335W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39901390:39901390(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2900C>T
AA Mutation p.Ala967Val(p.A967V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39864488:39864488(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs6919807
CDS Mutation c.314G>A
AA Mutation p.Arg105His(p.R105H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39878488:39878488(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs192352327
CDS Mutation c.1445C>T
AA Mutation p.Thr482Met(p.T482M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39891407:39891407(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776017051
CDS Mutation c.2212C>T
AA Mutation p.Arg738Trp(p.R738W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000274867
Start 39898936:39898936(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2678T>C
AA Mutation p.Val893Ala(p.V893A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39901915:39901915(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3085G>C
AA Mutation p.Ala1029Pro(p.A1029P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39873337:39873337(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1144C>A
AA Mutation p.His382Asn(p.H382N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39901326:39901326(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs555209855
CDS Mutation c.2836G>A
AA Mutation p.Gly946Arg(p.G946R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39875408:39875408(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762109044
CDS Mutation c.1241G>A
AA Mutation p.Arg414Gln(p.R414Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39873306:39873306(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1113G>T
AA Mutation p.Glu371Asp(p.E371D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39901359:39901359(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2869T>G
AA Mutation p.Phe957Val(p.F957V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39864484:39864484(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.310G>A
AA Mutation p.Asp104Asn(p.D104N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39900126:39900126(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2729T>C
AA Mutation p.Val910Ala(p.V910A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39875375:39875375(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs533527149
CDS Mutation c.1208G>A
AA Mutation p.Arg403His(p.R403H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39883980:39883980(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773228065
CDS Mutation c.1864G>A
AA Mutation p.Val622Ile(p.V622I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000274867
Start 39896843:39896843(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2373C>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000274867
Start 39887545:39887545(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2013G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000274867
Start 39879201:39879201(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1569A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000274867
Start 39856452:39856452(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756332066
CDS Mutation c.150C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000274867
Start 39871521:39871521(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs531101009
CDS Mutation c.993C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000274867
Start 39897190:39897190(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2526C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000274867
Start 39901914:39901914(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773772935
CDS Mutation c.3084G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000274867
Start 39901950:39901950(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745497621
CDS Mutation c.3120A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000274867
Start 39867618:39867618(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.537C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence frameshift_variant
Transcription ID ENST00000274867
Start 39879202:39879202(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1574delC
AA Mutation p.Pro525LeufsTer11(p.P525Lfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 35
Mutation Consequence stop_gained
Transcription ID ENST00000274867
Start 39868844:39868844(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.784C>T
AA Mutation p.Arg262Ter(p.R262*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> DAAM2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39878535:39878535(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375733561
CDS Mutation c.1492C>T
AA Mutation p.Arg498Cys(p.R498C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39878215:39878215(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1314G>T
AA Mutation p.Glu438Asp(p.E438D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39900095:39900095(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2698C>T
AA Mutation p.Arg900Cys(p.R900C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39901305:39901305(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778845214
CDS Mutation c.2815G>A
AA Mutation p.Ala939Thr(p.A939T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39879422:39879422(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs181701991
CDS Mutation c.1790G>A
AA Mutation p.Arg597His(p.R597H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39901852:39901852(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs573237647
CDS Mutation c.3022C>T
AA Mutation p.Arg1008Trp(p.R1008W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39879358:39879358(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746541722
CDS Mutation c.1726G>A
AA Mutation p.Gly576Ser(p.G576S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39864501:39864501(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.327G>T
AA Mutation p.Met109Ile(p.M109I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39856313:39856313(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775379327
CDS Mutation c.11G>A
AA Mutation p.Arg4His(p.R4H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39901361:39901361(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2871C>A
AA Mutation p.Phe957Leu(p.F957L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39902023:39902023(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775538347
CDS Mutation c.3193C>T
AA Mutation p.Arg1065Trp(p.R1065W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000274867
Start 39878204:39878204(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1303C>T
AA Mutation p.Leu435Phe(p.L435F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000274867
Start 39891356:39891356(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2161C>A
AA Mutation p.Pro721Thr(p.P721T)
Mutation Classification Missense_Mutation
Feature Type Transcript