Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PLXNA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208042242:208042242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745341868
CDS Mutation	c.4142G>A
AA Mutation	p.Arg1381His(p.R1381H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208028085:208028085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563402733
CDS Mutation	c.5513G>A
AA Mutation	p.Arg1838His(p.R1838H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208033335:208033335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5039G>A
AA Mutation	p.Arg1680Gln(p.R1680Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208031599:208031599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5216A>G
AA Mutation	p.Lys1739Arg(p.K1739R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208044691:208044691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3691G>A
AA Mutation	p.Asp1231Asn(p.D1231N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208038438:208038438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4697A>G
AA Mutation	p.Gln1566Arg(p.Q1566R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208142424:208142424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147945367
CDS Mutation	c.1411G>A
AA Mutation	p.Glu471Lys(p.E471K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208216839:208216839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1084G>A
AA Mutation	p.Ala362Thr(p.A362T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208217726:208217726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.197C>T
AA Mutation	p.Ala66Val(p.A66V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208054507:208054507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548975568
CDS Mutation	c.2770G>A
AA Mutation	p.Gly924Arg(p.G924R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208217699:208217699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224G>A
AA Mutation	p.Gly75Asp(p.G75D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208042144:208042144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748477176
CDS Mutation	c.4240G>A
AA Mutation	p.Asp1414Asn(p.D1414N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208042195:208042195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771610537
CDS Mutation	c.4189C>T
AA Mutation	p.Arg1397Cys(p.R1397C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208092851:208092851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2032C>T
AA Mutation	p.Arg678Cys(p.R678C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208217429:208217429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774922495
CDS Mutation	c.494C>T
AA Mutation	p.Thr165Met(p.T165M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208043185:208043185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372372428
CDS Mutation	c.3893C>T
AA Mutation	p.Thr1298Met(p.T1298M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208060830:208060830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2594C>T
AA Mutation	p.Thr865Met(p.T865M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208052409:208052409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2911A>G
AA Mutation	p.Met971Val(p.M971V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208217088:208217088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772097656
CDS Mutation	c.835C>T
AA Mutation	p.Arg279Cys(p.R279C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208054471:208054471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770455227
CDS Mutation	c.2806G>A
AA Mutation	p.Glu936Lys(p.E936K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208044532:208044532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3850C>T
AA Mutation	p.Arg1284Cys(p.R1284C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208217705:208217705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.218T>G
AA Mutation	p.Leu73Arg(p.L73R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208042243:208042243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4141C>T
AA Mutation	p.Arg1381Cys(p.R1381C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208028021:208028021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5577G>C
AA Mutation	p.Lys1859Asn(p.K1859N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367033
Start	208210304:208210304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1347G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367033
Start	208079269:208079269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2577A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367033
Start	208039762:208039762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559463221
CDS Mutation	c.4359C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367033
Start	208038973:208038973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113860539
CDS Mutation	c.4512C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367033
Start	208210337:208210337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779560632
CDS Mutation	c.1314C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367033
Start	208210319:208210319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759135591
CDS Mutation	c.1332C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367033
Start	208046058:208046058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3315C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367033
Start	208142425:208142425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374407002
CDS Mutation	c.1410C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367033
Start	208217742:208217742(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.181delG
AA Mutation	p.Ala61ProfsTer13(p.A61Pfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367033
Start	208027283:208027283(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5645delA
AA Mutation	p.Lys1882ArgfsTer40(p.K1882Rfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367033
Start	208217536:208217537(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.386dupG
AA Mutation	p.Cys129TrpfsTer16(p.C129Wfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000367033
Start	208045102:208045103(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3603_3604insAGAAGA
AA Mutation	p.Cys1201_Glu1202insArgArg(p.C1201_E1202insRR)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PLXNA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208044562:208044562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3820C>G
AA Mutation	p.Leu1274Val(p.L1274V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208038468:208038468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200636622
CDS Mutation	c.4667G>A
AA Mutation	p.Arg1556His(p.R1556H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208044664:208044664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746253674
CDS Mutation	c.3718G>A
AA Mutation	p.Val1240Ile(p.V1240I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367033
Start	208084400:208084400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749597067
CDS Mutation	c.2278G>A
AA Mutation	p.Val760Ile(p.V760I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000367033
Start	208060801:208060801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754005837
CDS Mutation	c.2623C>T
AA Mutation	p.Arg875Ter(p.R875*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000367033
Start	208098926:208098926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1651C>T
AA Mutation	p.Arg551Ter(p.R551*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript