Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DOCK3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51354897:51354897(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4123T>C
AA Mutation p.Cys1375Arg(p.C1375R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51362597:51362597(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5216G>A
AA Mutation p.Ser1739Asn(p.S1739N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51089256:51089256(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377200419
CDS Mutation c.563G>A
AA Mutation p.Arg188Gln(p.R188Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51275168:51275168(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2638C>T
AA Mutation p.Leu880Phe(p.L880F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51333189:51333189(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3547C>T
AA Mutation p.Arg1183Cys(p.R1183C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51090326:51090326(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.688G>A
AA Mutation p.Gly230Arg(p.G230R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51270914:51270914(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2455A>T
AA Mutation p.Met819Leu(p.M819L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000266037
Start 51090231:51090231(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.593T>C
AA Mutation p.Val198Ala(p.V198A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51090265:51090265(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.627T>G
AA Mutation p.Cys209Trp(p.C209W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51312569:51312569(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3187C>G
AA Mutation p.Leu1063Val(p.L1063V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51236405:51236405(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1978G>A
AA Mutation p.Gly660Ser(p.G660S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51227401:51227401(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1496G>A
AA Mutation p.Arg499Gln(p.R499Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51225700:51225700(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1304G>A
AA Mutation p.Arg435Lys(p.R435K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000266037
Start 51380127:51380127(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5503C>A
AA Mutation p.His1835Asn(p.H1835N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51354894:51354894(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4120G>T
AA Mutation p.Val1374Leu(p.V1374L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51090333:51090333(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.695A>G
AA Mutation p.Asp232Gly(p.D232G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51277725:51277725(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2794C>T
AA Mutation p.Arg932Trp(p.R932W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51315057:51315057(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774398189
CDS Mutation c.3331C>T
AA Mutation p.Arg1111Trp(p.R1111W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51208821:51208821(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1085G>A
AA Mutation p.Arg362Gln(p.R362Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 50841699:50841699(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.146A>C
AA Mutation p.Lys49Thr(p.K49T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51381327:51381327(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782707574
CDS Mutation c.5861G>A
AA Mutation p.Arg1954Gln(p.R1954Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51227407:51227407(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1502G>A
AA Mutation p.Arg501Gln(p.R501Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51277696:51277696(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2765C>T
AA Mutation p.Ser922Leu(p.S922L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51310252:51310252(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2943T>G
AA Mutation p.Phe981Leu(p.F981L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000266037
Start 51361997:51361997(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5145G>T
AA Mutation p.Gln1715His(p.Q1715H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51064584:51064584(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs570454630
CDS Mutation c.452A>G
AA Mutation p.Asp151Gly(p.D151G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51315099:51315099(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3373G>A
AA Mutation p.Glu1125Lys(p.E1125K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000266037
Start 51381349:51381349(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5883C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000266037
Start 51236404:51236404(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1977C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000266037
Start 51362586:51362586(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369636952
CDS Mutation c.5205G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000266037
Start 51277736:51277736(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2805G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000266037
Start 51315119:51315119(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3393C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000266037
Start 51090286:51090286(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.648C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000266037
Start 51228007:51228007(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1566C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000266037
Start 51277658:51277658(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781656330
CDS Mutation c.2727C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence frameshift_variant
Transcription ID ENST00000266037
Start 51380173:51380173(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs782665429
CDS Mutation c.5555delC
AA Mutation p.Pro1852GlnfsTer45(p.P1852Qfs*45)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 37
Mutation Consequence frameshift_variant
Transcription ID ENST00000266037
Start 51380173:51380174(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5554_5555delCC
AA Mutation p.Pro1852SerfsTer46(p.P1852Sfs*46)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 38
Mutation Consequence frameshift_variant
Transcription ID ENST00000266037
Start 51381075:51381075(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5613delC
AA Mutation p.Thr1872GlnfsTer25(p.T1872Qfs*25)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> DOCK3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51361915:51361915(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778025492
CDS Mutation c.5063C>T
AA Mutation p.Ala1688Val(p.A1688V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51208821:51208821(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1085G>A
AA Mutation p.Arg362Gln(p.R362Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51064550:51064550(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754707449
CDS Mutation c.418C>T
AA Mutation p.Arg140Trp(p.R140W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51090346:51090346(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.708C>A
AA Mutation p.Phe236Leu(p.F236L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51277725:51277725(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2794C>T
AA Mutation p.Arg932Trp(p.R932W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51270944:51270944(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769251462
CDS Mutation c.2485A>G
AA Mutation p.Met829Val(p.M829V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51075426:51075426(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.535G>T
AA Mutation p.Asp179Tyr(p.D179Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51160679:51160679(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1014G>T
AA Mutation p.Lys338Asn(p.K338N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51227432:51227432(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1527C>A
AA Mutation p.Phe509Leu(p.F509L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51275097:51275097(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2567T>G
AA Mutation p.Leu856Arg(p.L856R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000266037
Start 51225747:51225747(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1351C>T
AA Mutation p.Leu451Phe(p.L451F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000266037
Start 51348936:51348936(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759476559
CDS Mutation c.4000C>T
AA Mutation p.Arg1334Trp(p.R1334W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000266037
Start 51228007:51228007(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1566C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000266037
Start 51381349:51381349(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5883C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000266037
Start 51159282:51159282(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200460488
CDS Mutation c.867C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000266037
Start 51225696:51225696(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1300G>T
AA Mutation p.Glu434Ter(p.E434*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000266037
Start 50934045:50934045(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.283G>T
AA Mutation p.Glu95Ter(p.E95*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript