Colon Cancer: Gene >> KIF13B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29188602:29188602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229G>T
AA Mutation	p.Asp77Tyr(p.D77Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29148616:29148616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1774G>T
AA Mutation	p.Ala592Ser(p.A592S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29130538:29130538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781387599
CDS Mutation	c.3070C>T
AA Mutation	p.Arg1024Trp(p.R1024W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29132378:29132378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2872G>A
AA Mutation	p.Asp958Asn(p.D958N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29072112:29072112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4726G>A
AA Mutation	p.Ala1576Thr(p.A1576T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29123418:29123418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766406923
CDS Mutation	c.3427G>A
AA Mutation	p.Ala1143Thr(p.A1143T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29132360:29132360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs12549991
CDS Mutation	c.2890G>A
AA Mutation	p.Ala964Thr(p.A964T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29132385:29132385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2865A>C
AA Mutation	p.Lys955Asn(p.K955N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29122626:29122626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3500A>C
AA Mutation	p.Glu1167Ala(p.E1167A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29072169:29072169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4669C>T
AA Mutation	p.Pro1557Ser(p.P1557S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29140113:29140113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2563G>A
AA Mutation	p.Ala855Thr(p.A855T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29075309:29075309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374209248
CDS Mutation	c.4493C>T
AA Mutation	p.Pro1498Leu(p.P1498L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29071625:29071625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5213C>T
AA Mutation	p.Pro1738Leu(p.P1738L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29191033:29191033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187T>C
AA Mutation	p.Trp63Arg(p.W63R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29109935:29109935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4066T>A
AA Mutation	p.Leu1356Ile(p.L1356I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29134201:29134201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2623C>A
AA Mutation	p.Leu875Met(p.L875M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29071719:29071719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5119G>A
AA Mutation	p.Val1707Ile(p.V1707I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29130607:29130607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3001A>G
AA Mutation	p.Asn1001Asp(p.N1001D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29176110:29176110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.903A>C
AA Mutation	p.Lys301Asn(p.K301N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29147510:29147510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763012855
CDS Mutation	c.1906G>A
AA Mutation	p.Glu636Lys(p.E636K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29155801:29155801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1460G>A
AA Mutation	p.Gly487Glu(p.G487E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29116859:29116859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3809G>T
AA Mutation	p.Arg1270Ile(p.R1270I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29177567:29177567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.732G>T
AA Mutation	p.Glu244Asp(p.E244D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524189
Start	29130551:29130551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773584257
CDS Mutation	c.3057A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524189
Start	29155767:29155767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752632859
CDS Mutation	c.1494G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524189
Start	29150335:29150335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1584T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524189
Start	29127194:29127194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3150T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524189
Start	29176128:29176128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.885T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524189
Start	29118934:29118934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544452612
CDS Mutation	c.3594G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000524189
Start	29113530:29113530(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3863delA
AA Mutation	p.Lys1288ArgfsTer13(p.K1288Rfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000524189
Start	29148733:29148733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1657C>T
AA Mutation	p.Arg553Ter(p.R553*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000524189
Start	29124124:29124124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3253-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> KIF13B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29109505:29109505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754322224
CDS Mutation	c.4090G>A
AA Mutation	p.Ala1364Thr(p.A1364T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29142198:29142198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2293G>A
AA Mutation	p.Asp765Asn(p.D765N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29110043:29110043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553766326
CDS Mutation	c.3958G>T
AA Mutation	p.Ala1320Ser(p.A1320S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29176116:29176116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.897G>T
AA Mutation	p.Lys299Asn(p.K299N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000524189
Start	29134206:29134206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2618A>T
AA Mutation	p.Lys873Ile(p.K873I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524189
Start	29116945:29116945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781722667
CDS Mutation	c.3723G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000524189
Start	29150384:29150384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1536-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript