Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DCLK1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 36125900:36125900(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.238C>T
AA Mutation p.Arg80Trp(p.R80W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35774593:35774593(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2165C>T
AA Mutation p.Ser722Leu(p.S722L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35822784:35822784(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1499A>G
AA Mutation p.Lys500Arg(p.K500R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35793432:35793432(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1992G>T
AA Mutation p.Lys664Asn(p.K664N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35871266:35871266(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.898G>A
AA Mutation p.Gly300Arg(p.G300R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35808297:35808297(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1790T>C
AA Mutation p.Leu597Pro(p.L597P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35839111:35839111(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1101G>T
AA Mutation p.Glu367Asp(p.E367D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35810943:35810943(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1580A>C
AA Mutation p.Lys527Thr(p.K527T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 36125945:36125945(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746085515
CDS Mutation c.193G>A
AA Mutation p.Gly65Arg(p.G65R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 36126005:36126005(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.133C>T
AA Mutation p.Arg45Cys(p.R45C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 36125992:36125992(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373107227
CDS Mutation c.146C>T
AA Mutation p.Thr49Met(p.T49M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 36125981:36125981(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.157G>A
AA Mutation p.Glu53Lys(p.E53K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35808268:35808268(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1819G>C
AA Mutation p.Asp607His(p.D607H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 36112086:36112086(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.506C>G
AA Mutation p.Ala169Gly(p.A169G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35774665:35774665(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2093G>A
AA Mutation p.Arg698Gln(p.R698Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000360631
Start 35828305:35828305(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773115614
CDS Mutation c.1232C>T
AA Mutation p.Ser411Leu(p.S411L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35836064:35836064(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1198A>C
AA Mutation p.Asn400His(p.N400H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 36111894:36111894(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.698G>A
AA Mutation p.Arg233His(p.R233H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35822830:35822830(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1453G>A
AA Mutation p.Glu485Lys(p.E485K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 36111949:36111949(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.643C>A
AA Mutation p.Gln215Lys(p.Q215K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35871254:35871254(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777971990
CDS Mutation c.910C>T
AA Mutation p.Arg304Cys(p.R304C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000360631
Start 36111980:36111980(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.612G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000360631
Start 35854532:35854532(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201566141
CDS Mutation c.1002A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000360631
Start 36111908:36111908(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150324103
CDS Mutation c.684G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000360631
Start 35822792:35822792(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772511864
CDS Mutation c.1491C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000360631
Start 35828304:35828304(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1233G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000360631
Start 35828304:35828304(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1233G>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000360631
Start 35793471:35793471(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1953C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000360631
Start 36126045:36126045(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.93G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000360631
Start 35793435:35793435(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1989A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000360631
Start 36125781:36125781(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776065878
CDS Mutation c.357C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000360631
Start 36125982:36125982(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749628821
CDS Mutation c.156C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000360631
Start 35839150:35839150(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1062G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence stop_gained
Transcription ID ENST00000360631
Start 36112063:36112063(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754197263
CDS Mutation c.529C>T
AA Mutation p.Arg177Ter(p.R177*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence stop_gained
Transcription ID ENST00000360631
Start 36125894:36125894(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778679656
CDS Mutation c.244C>T
AA Mutation p.Arg82Ter(p.R82*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence stop_gained
Transcription ID ENST00000360631
Start 35774666:35774666(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2092C>T
AA Mutation p.Arg698Ter(p.R698*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence stop_gained
Transcription ID ENST00000360631
Start 35805740:35805740(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1903C>T
AA Mutation p.Arg635Ter(p.R635*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> DCLK1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35774558:35774558(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745824879
CDS Mutation c.2200C>T
AA Mutation p.Arg734Cys(p.R734C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35810957:35810957(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1566C>A
AA Mutation p.His522Gln(p.H522Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35774545:35774545(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2213C>T
AA Mutation p.Ser738Leu(p.S738L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35774635:35774635(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757007588
CDS Mutation c.2123G>A
AA Mutation p.Arg708Gln(p.R708Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35774597:35774597(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2161G>A
AA Mutation p.Glu721Lys(p.E721K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35793376:35793376(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2048C>A
AA Mutation p.Ser683Tyr(p.S683Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 35822828:35822828(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1455G>T
AA Mutation p.Glu485Asp(p.E485D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000360631
Start 36125864:36125864(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.274A>C
AA Mutation p.Thr92Pro(p.T92P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000360631
Start 36112061:36112061(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.531A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000360631
Start 35774625:35774625(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377204170
CDS Mutation c.2133G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000360631
Start 35809085:35809085(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1699A>T
AA Mutation p.Lys567Ter(p.K567*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript