Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KIF26B

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245685820:245685820(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2837C>A
AA Mutation p.Pro946His(p.P946H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245646133:245646133(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757742040
CDS Mutation c.2111G>A
AA Mutation p.Arg704His(p.R704H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245686629:245686629(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766451582
CDS Mutation c.3646G>A
AA Mutation p.Asp1216Asn(p.D1216N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245156403:245156403(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.185C>T
AA Mutation p.Ala62Val(p.A62V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245684316:245684316(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145521032
CDS Mutation c.2342C>T
AA Mutation p.Ala781Val(p.A781V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245602592:245602592(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1366C>T
AA Mutation p.Arg456Cys(p.R456C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245684246:245684246(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769468332
CDS Mutation c.2272G>A
AA Mutation p.Ala758Thr(p.A758T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245687991:245687991(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5008G>A
AA Mutation p.Gly1670Ser(p.G1670S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245688756:245688756(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5773G>A
AA Mutation p.Val1925Met(p.V1925M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245602681:245602681(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1455T>G
AA Mutation p.Asp485Glu(p.D485E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245686801:245686801(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3818G>T
AA Mutation p.Ser1273Ile(p.S1273I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245687250:245687250(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4267T>A
AA Mutation p.Ser1423Thr(p.S1423T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245684301:245684301(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760715594
CDS Mutation c.2327C>T
AA Mutation p.Ala776Val(p.A776V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245698189:245698189(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200288645
CDS Mutation c.5908C>T
AA Mutation p.Arg1970Cys(p.R1970C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245686324:245686324(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771122784
CDS Mutation c.3341C>T
AA Mutation p.Ala1114Val(p.A1114V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245688741:245688741(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774653307
CDS Mutation c.5758G>A
AA Mutation p.Glu1920Lys(p.E1920K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245684277:245684277(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2303T>C
AA Mutation p.Met768Thr(p.M768T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245687187:245687187(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs184020024
CDS Mutation c.4204C>T
AA Mutation p.Arg1402Trp(p.R1402W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245366909:245366909(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.541G>A
AA Mutation p.Asp181Asn(p.D181N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245698923:245698923(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6064G>A
AA Mutation p.Glu2022Lys(p.E2022K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245367129:245367129(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.761C>T
AA Mutation p.Thr254Ile(p.T254I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245611836:245611836(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1958C>T
AA Mutation p.Ala653Val(p.A653V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245686462:245686462(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3479C>T
AA Mutation p.Thr1160Ile(p.T1160I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245367116:245367116(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371419440
CDS Mutation c.748G>A
AA Mutation p.Ala250Thr(p.A250T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245688072:245688072(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5089G>A
AA Mutation p.Ala1697Thr(p.A1697T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245366996:245366996(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs532207390
CDS Mutation c.628G>A
AA Mutation p.Gly210Ser(p.G210S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245540937:245540937(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772241455
CDS Mutation c.1337C>T
AA Mutation p.Pro446Leu(p.P446L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245686083:245686083(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs567573827
CDS Mutation c.3100G>A
AA Mutation p.Ala1034Thr(p.A1034T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245688771:245688771(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5788C>T
AA Mutation p.Arg1930Trp(p.R1930W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245685790:245685790(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2807T>C
AA Mutation p.Ile936Thr(p.I936T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245687148:245687148(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4165A>G
AA Mutation p.Thr1389Ala(p.T1389A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245698965:245698965(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200981354
CDS Mutation c.6106G>A
AA Mutation p.Glu2036Lys(p.E2036K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245686725:245686725(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371194278
CDS Mutation c.3742G>A
AA Mutation p.Val1248Ile(p.V1248I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245702583:245702583(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761880773
CDS Mutation c.6304G>A
AA Mutation p.Asp2102Asn(p.D2102N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245367074:245367074(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369084969
CDS Mutation c.706G>A
AA Mutation p.Val236Met(p.V236M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245540810:245540810(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1210C>T
AA Mutation p.Arg404Trp(p.R404W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245609314:245609314(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1700G>A
AA Mutation p.Gly567Asp(p.G567D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245611888:245611888(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2010C>A
AA Mutation p.Asp670Glu(p.D670E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245686015:245686015(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767436618
CDS Mutation c.3032C>T
AA Mutation p.Ala1011Val(p.A1011V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245156406:245156406(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.188T>G
AA Mutation p.Leu63Arg(p.L63R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245698946:245698946(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201847058
CDS Mutation c.6087C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245686280:245686280(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200052878
CDS Mutation c.3297G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245687453:245687453(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4470C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245686595:245686595(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746673858
CDS Mutation c.3612C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245685791:245685791(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745847923
CDS Mutation c.2808C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245685893:245685893(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2910G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245685539:245685539(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762404121
CDS Mutation c.2556C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245685800:245685800(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760386992
CDS Mutation c.2817C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245540827:245540827(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372159973
CDS Mutation c.1227C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245685962:245685962(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2979C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245602753:245602753(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1527C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 52
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245686307:245686307(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777236887
CDS Mutation c.3324C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245687696:245687696(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs569587548
CDS Mutation c.4713G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245698958:245698958(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755672216
CDS Mutation c.6099G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 55
Mutation Consequence frameshift_variant
Transcription ID ENST00000407071
Start 245688480:245688480(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5503delG
AA Mutation p.Ala1835ProfsTer41(p.A1835Pfs*41)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 56
Mutation Consequence frameshift_variant
Transcription ID ENST00000407071
Start 245686177:245686177(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3199delC
AA Mutation p.Arg1067GlyfsTer65(p.R1067Gfs*65)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 57
Mutation Consequence stop_gained
Transcription ID ENST00000407071
Start 245602664:245602664(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1438C>T
AA Mutation p.Gln480Ter(p.Q480*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 58
Mutation Consequence frameshift_variant
Transcription ID ENST00000407071
Start 245646258:245646259(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2236_2237insAGAT
AA Mutation p.Gly746GlufsTer98(p.G746Efs*98)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> KIF26B

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245687188:245687188(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200347978
CDS Mutation c.4205G>A
AA Mutation p.Arg1402Gln(p.R1402Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245602593:245602593(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1367G>A
AA Mutation p.Arg456His(p.R456H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245685519:245685519(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200467850
CDS Mutation c.2536G>A
AA Mutation p.Ala846Thr(p.A846T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245686356:245686356(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3373C>T
AA Mutation p.Arg1125Cys(p.R1125C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245367318:245367318(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.950G>A
AA Mutation p.Gly317Asp(p.G317D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245702598:245702598(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201648182
CDS Mutation c.6319C>T
AA Mutation p.Arg2107Cys(p.R2107C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245686232:245686232(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3249C>A
AA Mutation p.Ser1083Arg(p.S1083R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245686876:245686876(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3893T>C
AA Mutation p.Phe1298Ser(p.F1298S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000407071
Start 245686877:245686877(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3894C>A
AA Mutation p.Phe1298Leu(p.F1298L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245685773:245685773(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2790G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245698991:245698991(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747577473
CDS Mutation c.6132G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245367322:245367322(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.954C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000407071
Start 245609273:245609273(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1659C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000407071
Start 245685426:245685426(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2446delG
AA Mutation p.Glu816ArgfsTer15(p.E816Rfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript