Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PLXNB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48422372:48422372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1378G>C
AA Mutation	p.Asp460His(p.D460H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48424199:48424199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.413G>A
AA Mutation	p.Gly138Glu(p.G138E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48413800:48413800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4405C>T
AA Mutation	p.Arg1469Cys(p.R1469C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48409396:48409396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755289308
CDS Mutation	c.6020C>T
AA Mutation	p.Ala2007Val(p.A2007V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48419708:48419708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374953457
CDS Mutation	c.2578G>A
AA Mutation	p.Ala860Thr(p.A860T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48418322:48418322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144428611
CDS Mutation	c.3091C>T
AA Mutation	p.Arg1031Cys(p.R1031C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48424214:48424214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760971221
CDS Mutation	c.398G>A
AA Mutation	p.Arg133Gln(p.R133Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48420031:48420031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2255G>C
AA Mutation	p.Gly752Ala(p.G752A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48419834:48419834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2452C>A
AA Mutation	p.Leu818Met(p.L818M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48412256:48412256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5082T>G
AA Mutation	p.Cys1694Trp(p.C1694W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48410471:48410471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5504C>T
AA Mutation	p.Thr1835Ile(p.T1835I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48423692:48423692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201285818
CDS Mutation	c.920G>A
AA Mutation	p.Arg307Gln(p.R307Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48424047:48424047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.565C>A
AA Mutation	p.Leu189Met(p.L189M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48418304:48418304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3109C>T
AA Mutation	p.Pro1037Ser(p.P1037S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48409421:48409421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5995G>A
AA Mutation	p.Val1999Met(p.V1999M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48413092:48413092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4613A>G
AA Mutation	p.Asp1538Gly(p.D1538G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48424287:48424287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325G>T
AA Mutation	p.Val109Leu(p.V109L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48419906:48419906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2380C>T
AA Mutation	p.Pro794Ser(p.P794S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48418488:48418488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3010G>A
AA Mutation	p.Ala1004Thr(p.A1004T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48412574:48412574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4901G>A
AA Mutation	p.Arg1634His(p.R1634H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48412595:48412595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746314397
CDS Mutation	c.4880G>A
AA Mutation	p.Arg1627His(p.R1627H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48418976:48418976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199581131
CDS Mutation	c.2896C>T
AA Mutation	p.Arg966Trp(p.R966W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48419881:48419881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2405C>A
AA Mutation	p.Pro802His(p.P802H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48418980:48418980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2892G>T
AA Mutation	p.Glu964Asp(p.E964D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296440
Start	48424258:48424258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.354C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296440
Start	48419838:48419838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2448G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296440
Start	48419613:48419613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751151140
CDS Mutation	c.2673C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296440
Start	48420952:48420952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138006677
CDS Mutation	c.1815C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296440
Start	48424213:48424213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.399G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296440
Start	48414946:48414946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4062A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296440
Start	48423909:48423909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296440
Start	48409726:48409726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5784C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296440
Start	48424076:48424076(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.536delG
AA Mutation	p.Gly179ValfsTer41(p.G179Vfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296440
Start	48419592:48419592(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2694delC
AA Mutation	p.Leu900SerfsTer25(p.L900Sfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000296440
Start	48421691:48421691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1636C>T
AA Mutation	p.Arg546Ter(p.R546*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296440
Start	48419712:48419713(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2573dupG
AA Mutation	p.Asp859Ter(p.D859*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PLXNB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296440
Start	48422157:48422157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1468T>C
AA Mutation	p.Ser490Pro(p.S490P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296440
Start	48411010:48411010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5274G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296440
Start	48420940:48420940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1827C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296440
Start	48412519:48412519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4956C>T
Mutation Classification	Silent
Feature Type	Transcript