Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PLXNA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154461294:154461294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790C>T
AA Mutation	p.Arg264Cys(p.R264C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154466697:154466697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3011C>T
AA Mutation	p.Ala1004Val(p.A1004V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154460449:154460449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148785068
CDS Mutation	c.266G>A
AA Mutation	p.Arg89His(p.R89H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154464063:154464063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1660C>T
AA Mutation	p.Pro554Ser(p.P554S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154468719:154468719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4277A>C
AA Mutation	p.Lys1426Thr(p.K1426T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154460434:154460434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782701104
CDS Mutation	c.251G>A
AA Mutation	p.Arg84His(p.R84H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154461501:154461501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199954840
CDS Mutation	c.997C>T
AA Mutation	p.Arg333Trp(p.R333W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154466676:154466676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2990G>T
AA Mutation	p.Ser997Ile(p.S997I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154461360:154461360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376086499
CDS Mutation	c.856G>A
AA Mutation	p.Gly286Ser(p.G286S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154462216:154462216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1223C>T
AA Mutation	p.Ala408Val(p.A408V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154465953:154465953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2551C>T
AA Mutation	p.Pro851Ser(p.P851S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154468830:154468830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4295C>T
AA Mutation	p.Ala1432Val(p.A1432V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154461148:154461148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781828247
CDS Mutation	c.644C>T
AA Mutation	p.Thr215Met(p.T215M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154467443:154467443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3413T>C
AA Mutation	p.Val1138Ala(p.V1138A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154460331:154460331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148G>T
AA Mutation	p.Val50Leu(p.V50L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154460332:154460332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.149T>G
AA Mutation	p.Val50Gly(p.V50G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154466421:154466421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782070642
CDS Mutation	c.2845G>A
AA Mutation	p.Gly949Arg(p.G949R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154466170:154466170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2699A>C
AA Mutation	p.Glu900Ala(p.E900A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154465720:154465720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2405G>A
AA Mutation	p.Arg802His(p.R802H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154460223:154460223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782271984
CDS Mutation	c.40G>A
AA Mutation	p.Val14Met(p.V14M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154460253:154460253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782215325
CDS Mutation	c.70C>T
AA Mutation	p.Arg24Cys(p.R24C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369682
Start	154463634:154463634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781978007
CDS Mutation	c.1491C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369682
Start	154468359:154468359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150847200
CDS Mutation	c.4020C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369682
Start	154471279:154471279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199507126
CDS Mutation	c.5331C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369682
Start	154467856:154467856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782275281
CDS Mutation	c.3675G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369682
Start	154465137:154465137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138065609
CDS Mutation	c.2163C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369682
Start	154468365:154468365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782050805
CDS Mutation	c.4026C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369682
Start	154467132:154467132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782401505
CDS Mutation	c.3183C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369682
Start	154464490:154464490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1917C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369682
Start	154471126:154471126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5178G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369682
Start	154466057:154466057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782464424
CDS Mutation	c.2655G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369682
Start	154460225:154460225(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs782361229
CDS Mutation	c.49delG
AA Mutation	p.Ala17ProfsTer12(p.A17Pfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369682
Start	154464823:154464823(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2002delC
AA Mutation	p.His668ThrfsTer26(p.H668Tfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369682
Start	154460224:154460225(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs782247826
CDS Mutation	c.49dupG
AA Mutation	p.Ala17GlyfsTer39(p.A17Gfs*39)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PLXNA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154468529:154468529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4190G>T
AA Mutation	p.Ser1397Ile(p.S1397I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154460373:154460373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150180614
CDS Mutation	c.190C>T
AA Mutation	p.Arg64Trp(p.R64W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154466221:154466221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2750A>G
AA Mutation	p.Asp917Gly(p.D917G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154467118:154467118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3169C>T
AA Mutation	p.Arg1057Cys(p.R1057C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369682
Start	154468955:154468955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4420G>T
AA Mutation	p.Asp1474Tyr(p.D1474Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369682
Start	154461200:154461200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377627483
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369682
Start	154471569:154471569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374284684
CDS Mutation	c.5451C>T
Mutation Classification	Silent
Feature Type	Transcript