Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DOCK11

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118643517:118643517(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4321C>A
AA Mutation p.Leu1441Ile(p.L1441I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118662769:118662769(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5053A>G
AA Mutation p.Met1685Val(p.M1685V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118580139:118580139(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755708340
CDS Mutation c.1555C>T
AA Mutation p.Arg519Cys(p.R519C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118654725:118654725(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4819T>G
AA Mutation p.Leu1607Val(p.L1607V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118566621:118566621(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.919T>A
AA Mutation p.Leu307Met(p.L307M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118578571:118578571(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1436C>T
AA Mutation p.Ala479Val(p.A479V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118573956:118573956(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1327G>A
AA Mutation p.Gly443Ser(p.G443S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118608076:118608076(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2686C>A
AA Mutation p.Leu896Ile(p.L896I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118561497:118561497(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.673G>A
AA Mutation p.Ala225Thr(p.A225T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118573867:118573867(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1238C>T
AA Mutation p.Ala413Val(p.A413V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118662742:118662742(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5026G>A
AA Mutation p.Glu1676Lys(p.E1676K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118543565:118543565(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.364T>C
AA Mutation p.Phe122Leu(p.F122L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118568106:118568106(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.979A>C
AA Mutation p.Lys327Gln(p.K327Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118593248:118593248(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2174A>T
AA Mutation p.Lys725Ile(p.K725I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118561463:118561463(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.639T>G
AA Mutation p.Asn213Lys(p.N213K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118573998:118573998(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1369C>G
AA Mutation p.Gln457Glu(p.Q457E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118545344:118545344(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.414G>T
AA Mutation p.Lys138Asn(p.K138N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118639479:118639479(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4046A>C
AA Mutation p.Lys1349Thr(p.K1349T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118681231:118681231(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5845G>T
AA Mutation p.Gly1949Cys(p.G1949C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118608306:118608306(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2827G>T
AA Mutation p.Ala943Ser(p.A943S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118627562:118627562(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3647G>T
AA Mutation p.Ser1216Ile(p.S1216I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000276202
Start 118546062:118546062(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.504A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000276202
Start 118608099:118608099(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2709C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000276202
Start 118681741:118681741(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5910C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000276202
Start 118662690:118662690(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4974A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000276202
Start 118610412:118610412(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3090C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000276202
Start 118578539:118578539(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1404G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000276202
Start 118615647:118615647(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3228C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence frameshift_variant
Transcription ID ENST00000276202
Start 118566153:118566153(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.848delA
AA Mutation p.Lys283ArgfsTer4(p.K283Rfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 30
Mutation Consequence stop_gained
Transcription ID ENST00000276202
Start 118624617:118624617(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3550C>T
AA Mutation p.Arg1184Ter(p.R1184*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence stop_gained
Transcription ID ENST00000276202
Start 118680557:118680557(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5536G>T
AA Mutation p.Glu1846Ter(p.E1846*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence stop_gained
Transcription ID ENST00000276202
Start 118561449:118561449(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.625A>T
AA Mutation p.Lys209Ter(p.K209*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000276202
Start 118676592:118676593(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.5322dupT
AA Mutation p.Glu1775Ter(p.E1775*)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 34
Mutation Consequence frameshift_variant
Transcription ID ENST00000276202
Start 118566152:118566153(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.848dupA
AA Mutation p.Glu284GlyfsTer9(p.E284Gfs*9)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> DOCK11

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118593270:118593270(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2196T>G
AA Mutation p.Phe732Leu(p.F732L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118649065:118649065(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4519C>A
AA Mutation p.Leu1507Ile(p.L1507I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118676011:118676011(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5275C>A
AA Mutation p.Leu1759Ile(p.L1759I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118681070:118681070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5684T>C
AA Mutation p.Phe1895Ser(p.F1895S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118561474:118561474(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768187628
CDS Mutation c.650C>T
AA Mutation p.Ser217Leu(p.S217L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118566118:118566118(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.807G>T
AA Mutation p.Lys269Asn(p.K269N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000276202
Start 118588248:118588248(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1907T>G
AA Mutation p.Phe636Cys(p.F636C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000276202
Start 118643465:118643465(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4269T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000276202
Start 118599192:118599192(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769614070
CDS Mutation c.2526G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000276202
Start 118610358:118610358(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3036G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000276202
Start 118618590:118618590(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3333G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000276202
Start 118680557:118680557(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5536G>T
AA Mutation p.Glu1846Ter(p.E1846*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence splice_donor_variant
Transcription ID ENST00000276202
Start 118681796:118681796(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5963+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 14
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000276202
Start 118542925:118542925(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.220-1G>C
Mutation Classification Splice_Site
Feature Type Transcript