Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KIF13A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17785611:17785611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3392C>T
AA Mutation	p.Ala1131Val(p.A1131V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17764736:17764736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4792G>T
AA Mutation	p.Gly1598Cys(p.G1598C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17771128:17771128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4567C>T
AA Mutation	p.Arg1523Cys(p.R1523C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17855459:17855459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs73726225
CDS Mutation	c.472C>T
AA Mutation	p.Arg158Trp(p.R158W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17800050:17800050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2518G>A
AA Mutation	p.Glu840Lys(p.E840K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000259711
Start	17837581:17837581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833C>T
AA Mutation	p.Ser278Leu(p.S278L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17831124:17831124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377226069
CDS Mutation	c.1378G>A
AA Mutation	p.Glu460Lys(p.E460K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17987423:17987423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.41C>A
AA Mutation	p.Pro14His(p.P14H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17836930:17836930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1103G>T
AA Mutation	p.Arg368Leu(p.R368L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17800002:17800002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547042809
CDS Mutation	c.2566G>A
AA Mutation	p.Val856Ile(p.V856I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17817192:17817192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753700328
CDS Mutation	c.1828C>G
AA Mutation	p.Leu610Val(p.L610V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17780749:17780749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3827C>T
AA Mutation	p.Ala1276Val(p.A1276V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17831171:17831171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1331A>G
AA Mutation	p.Asp444Gly(p.D444G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17804475:17804475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2340C>A
AA Mutation	p.Phe780Leu(p.F780L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17779677:17779677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751899598
CDS Mutation	c.3854C>T
AA Mutation	p.Thr1285Met(p.T1285M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17780791:17780791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3785A>G
AA Mutation	p.His1262Arg(p.H1262R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17826068:17826068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1589G>A
AA Mutation	p.Arg530Gln(p.R530Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17817053:17817053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768744386
CDS Mutation	c.1967C>T
AA Mutation	p.Ala656Val(p.A656V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17849446:17849446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775888626
CDS Mutation	c.761C>T
AA Mutation	p.Ala254Val(p.A254V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259711
Start	17855613:17855613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189079716
CDS Mutation	c.318G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259711
Start	17799341:17799341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2715C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259711
Start	17781255:17781255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3591C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259711
Start	17787822:17787822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3315A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259711
Start	17764926:17764926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4602T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259711
Start	17804436:17804436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116064372
CDS Mutation	c.2379G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000259711
Start	17837077:17837077(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.956delG
AA Mutation	p.Gly319AlafsTer7(p.G319Afs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000259711
Start	17826040:17826040(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1617delT
AA Mutation	p.Phe539LeufsTer3(p.F539Lfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000259711
Start	17787792:17787792(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3345delA
AA Mutation	p.Val1116SerfsTer23(p.V1116Sfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000259711
Start	17804490:17804490(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2325delA
AA Mutation	p.Lys775AsnfsTer30(p.K775Nfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000259711
Start	17825909:17825909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1645C>T
AA Mutation	p.Arg549Ter(p.R549*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000259711
Start	17852020:17852020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517C>T
AA Mutation	p.Arg173Ter(p.R173*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000259711
Start	17764891:17764891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4637C>A
AA Mutation	p.Ser1546Ter(p.S1546*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000259711
Start	17794251:17794251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3220C>T
AA Mutation	p.Gln1074Ter(p.Q1074*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000259711
Start	17787791:17787792(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3345dupA
AA Mutation	p.Val1116SerfsTer4(p.V1116Sfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000259711
Start	17833960:17833960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1266+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> KIF13A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17849417:17849417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.790G>A
AA Mutation	p.Ala264Thr(p.A264T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17764905:17764905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4623G>T
AA Mutation	p.Arg1541Ser(p.R1541S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259711
Start	17778970:17778970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4069C>A
AA Mutation	p.Leu1357Met(p.L1357M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259711
Start	17764647:17764647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56327112
CDS Mutation	c.4881G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000259711
Start	17856117:17856117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226G>T
AA Mutation	p.Glu76Ter(p.E76*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript