Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KIF1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10261960:10261960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.419A>G
AA Mutation	p.Tyr140Cys(p.Y140C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10352649:10352649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3968C>A
AA Mutation	p.Pro1323His(p.P1323H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10258629:10258629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.320T>C
AA Mutation	p.Met107Thr(p.M107T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10296659:10296659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752648536
CDS Mutation	c.1855C>T
AA Mutation	p.Arg619Cys(p.R619C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10334587:10334587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2992G>C
AA Mutation	p.Glu998Gln(p.E998Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10361776:10361776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143800192
CDS Mutation	c.4255C>T
AA Mutation	p.Arg1419Cys(p.R1419C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10296993:10296993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1958C>G
AA Mutation	p.Pro653Arg(p.P653R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10279111:10279111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1195G>A
AA Mutation	p.Asp399Asn(p.D399N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10371165:10371165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765259892
CDS Mutation	c.4849C>T
AA Mutation	p.Arg1617Trp(p.R1617W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10297028:10297028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1993G>A
AA Mutation	p.Glu665Lys(p.E665K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10282333:10282333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1234T>G
AA Mutation	p.Phe412Val(p.F412V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10297072:10297072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2037G>T
AA Mutation	p.Glu679Asp(p.E679D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10324847:10324847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2627G>A
AA Mutation	p.Gly876Asp(p.G876D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10296903:10296903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1868G>A
AA Mutation	p.Arg623His(p.R623H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10375033:10375033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5276A>G
AA Mutation	p.Gln1759Arg(p.Q1759R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10368524:10368524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769092155
CDS Mutation	c.4810G>A
AA Mutation	p.Val1604Ile(p.V1604I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10324868:10324868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2648G>A
AA Mutation	p.Arg883Gln(p.R883Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10376577:10376577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761319935
CDS Mutation	c.5441C>T
AA Mutation	p.Ser1814Leu(p.S1814L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10363305:10363305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4327G>A
AA Mutation	p.Glu1443Lys(p.E1443K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10323990:10323990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766572494
CDS Mutation	c.2465G>A
AA Mutation	p.Arg822His(p.R822H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10258635:10258635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326G>T
AA Mutation	p.Gly109Val(p.G109V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377086
Start	10376569:10376569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768290105
CDS Mutation	c.5433G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377086
Start	10363292:10363292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4314C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377086
Start	10326126:10326126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566526002
CDS Mutation	c.2691C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377086
Start	10375031:10375031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5274G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377086
Start	10374349:10374349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4980C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377086
Start	10368523:10368523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749686737
CDS Mutation	c.4809C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377086
Start	10297003:10297003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1968T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377086
Start	10282476:10282476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1377T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377086
Start	10326321:10326321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763515223
CDS Mutation	c.2886G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377086
Start	10361031:10361031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116302604
CDS Mutation	c.4158G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377086
Start	10337438:10337438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3327C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377086
Start	10258615:10258615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377086
Start	10278052:10278052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1104G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377086
Start	10267454:10267454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.504G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377086
Start	10278037:10278037(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1092delC
AA Mutation	p.Asn365MetfsTer8(p.N365Mfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	stop_gained
Transcription ID	ENST00000377086
Start	10374407:10374407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5038C>T
AA Mutation	p.Arg1680Ter(p.R1680*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KIF1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10258659:10258659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350G>A
AA Mutation	p.Gly117Asp(p.G117D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10323990:10323990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766572494
CDS Mutation	c.2465G>A
AA Mutation	p.Arg822His(p.R822H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10258535:10258535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.226G>T
AA Mutation	p.Asp76Tyr(p.D76Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377086
Start	10296903:10296903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1868G>A
AA Mutation	p.Arg623His(p.R623H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377086
Start	10365609:10365609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750386624
CDS Mutation	c.4713C>T
Mutation Classification	Silent
Feature Type	Transcript