Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PLXNC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94220110:94220110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1649G>A
AA Mutation	p.Ser550Asn(p.S550N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000258526
Start	94248410:94248410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775083313
CDS Mutation	c.2776C>T
AA Mutation	p.Arg926Trp(p.R926W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94248335:94248335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2701G>T
AA Mutation	p.Asp901Tyr(p.D901Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94305248:94305248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4670T>G
AA Mutation	p.Val1557Gly(p.V1557G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94279527:94279527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756645590
CDS Mutation	c.3653G>A
AA Mutation	p.Arg1218Gln(p.R1218Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94247942:94247942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2428G>T
AA Mutation	p.Ala810Ser(p.A810S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94149561:94149561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.590C>T
AA Mutation	p.Ala197Val(p.A197V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94265113:94265113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3485C>T
AA Mutation	p.Thr1162Met(p.T1162M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94247969:94247969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773924211
CDS Mutation	c.2455C>T
AA Mutation	p.Arg819Cys(p.R819C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94240531:94240531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2167C>A
AA Mutation	p.Leu723Ile(p.L723I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94149768:94149768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797G>A
AA Mutation	p.Arg266His(p.R266H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94265155:94265155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3527T>G
AA Mutation	p.Ile1176Ser(p.I1176S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94298753:94298753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4196A>C
AA Mutation	p.Lys1399Thr(p.K1399T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94149686:94149686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.715C>A
AA Mutation	p.Leu239Ile(p.L239I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94237748:94237748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763485097
CDS Mutation	c.2065C>T
AA Mutation	p.Arg689Trp(p.R689W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94227170:94227170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774313920
CDS Mutation	c.1915G>A
AA Mutation	p.Glu639Lys(p.E639K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94304034:94304034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150282069
CDS Mutation	c.4585G>A
AA Mutation	p.Val1529Ile(p.V1529I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94248054:94248054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751117319
CDS Mutation	c.2540C>T
AA Mutation	p.Thr847Met(p.T847M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258526
Start	94149766:94149766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.795G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258526
Start	94224301:94224301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1776C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258526
Start	94298682:94298682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4125A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258526
Start	94247974:94247974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778989864
CDS Mutation	c.2460G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258526
Start	94149655:94149655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747904592
CDS Mutation	c.684C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258526
Start	94169227:94169227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1137T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258526
Start	94169236:94169236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772151160
CDS Mutation	c.1146C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258526
Start	94186450:94186450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745637999
CDS Mutation	c.1416C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258526
Start	94247936:94247936(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2426delT
AA Mutation	p.Leu809Ter(p.L809*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258526
Start	94298749:94298749(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4198delA
AA Mutation	p.Ile1400SerfsTer21(p.I1400Sfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000258526
Start	94279577:94279577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3703G>T
AA Mutation	p.Glu1235Ter(p.E1235*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258526
Start	94209658:94209659(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1514dupA
AA Mutation	p.Cys506ValfsTer3(p.C506Vfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258526
Start	94248333:94248334(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2699_2700insG
AA Mutation	p.Asp901ArgfsTer10(p.D901Rfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000258526
Start	94181445:94181445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1204-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PLXNC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94169189:94169189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779819475
CDS Mutation	c.1099G>A
AA Mutation	p.Ala367Thr(p.A367T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000258526
Start	94248411:94248411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753617960
CDS Mutation	c.2777G>A
AA Mutation	p.Arg926Gln(p.R926Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94186419:94186419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748183392
CDS Mutation	c.1385C>T
AA Mutation	p.Ser462Leu(p.S462L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94279484:94279484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139894368
CDS Mutation	c.3610G>A
AA Mutation	p.Val1204Ile(p.V1204I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94227218:94227218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1963A>G
AA Mutation	p.Thr655Ala(p.T655A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94255217:94255217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3008A>G
AA Mutation	p.Lys1003Arg(p.K1003R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000258526
Start	94259683:94259683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3200T>C
AA Mutation	p.Val1067Ala(p.V1067A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258526
Start	94209614:94209614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1464A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258526
Start	94294512:94294512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3906C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000258526
Start	94304053:94304053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4602+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript