Colon Cancer: Gene >> KIF14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200569979:200569979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3593G>T
AA Mutation	p.Arg1198Ile(p.R1198I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200614367:200614367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1406G>T
AA Mutation	p.Arg469Ile(p.R469I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200618275:200618275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.449A>G
AA Mutation	p.Glu150Gly(p.E150G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200618348:200618348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780290398
CDS Mutation	c.376A>G
AA Mutation	p.Lys126Glu(p.K126E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200565624:200565624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3707C>T
AA Mutation	p.Ser1236Phe(p.S1236F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200618535:200618535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.189A>G
AA Mutation	p.Ile63Met(p.I63M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200560836:200560836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753019306
CDS Mutation	c.4116G>T
AA Mutation	p.Lys1372Asn(p.K1372N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200592203:200592203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2690G>T
AA Mutation	p.Arg897Ile(p.R897I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200593759:200593759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2560A>C
AA Mutation	p.Asn854His(p.N854H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200603909:200603909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373895990
CDS Mutation	c.1793G>A
AA Mutation	p.Arg598Gln(p.R598Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200608907:200608907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771409397
CDS Mutation	c.1477A>G
AA Mutation	p.Ser493Gly(p.S493G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367350
Start	200592166:200592166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2727G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367350
Start	200560766:200560766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367350
Start	200601912:200601912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145353826
CDS Mutation	c.2136C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367350
Start	200560794:200560794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4158G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000367350
Start	200554591:200554591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4444C>T
AA Mutation	p.Gln1482Ter(p.Q1482*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000367350
Start	200600103:200600103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2311G>T
AA Mutation	p.Glu771Ter(p.E771*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000367350
Start	200605895:200605895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1608-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> KIF14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200614377:200614377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1396A>C
AA Mutation	p.Ile466Leu(p.I466L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200618015:200618015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.709A>G
AA Mutation	p.Thr237Ala(p.T237A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200565573:200565573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3758T>G
AA Mutation	p.Phe1253Cys(p.F1253C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200603909:200603909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373895990
CDS Mutation	c.1793G>A
AA Mutation	p.Arg598Gln(p.R598Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200605360:200605360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371145728
CDS Mutation	c.1669G>A
AA Mutation	p.Ala557Thr(p.A557T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200608881:200608881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1503A>C
AA Mutation	p.Lys501Asn(p.K501N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200565100:200565100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4040A>C
AA Mutation	p.Lys1347Thr(p.K1347T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367350
Start	200617771:200617771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.953A>C
AA Mutation	p.Lys318Thr(p.K318T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367350
Start	200554502:200554502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4533G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367350
Start	200560827:200560827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4125C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000367350
Start	200589218:200589218(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3113delA
AA Mutation	p.Gln1038ArgfsTer3(p.Q1038Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000367350
Start	200555445:200555445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4363G>T
AA Mutation	p.Glu1455Ter(p.E1455*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript