Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PREX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48658185:48658185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1925A>C
AA Mutation	p.Lys642Thr(p.K642T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48745093:48745093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145026241
CDS Mutation	c.346G>A
AA Mutation	p.Ala116Thr(p.A116T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48747867:48747867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371419352
CDS Mutation	c.233G>A
AA Mutation	p.Arg78His(p.R78H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48636584:48636584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150328810
CDS Mutation	c.4046G>A
AA Mutation	p.Arg1349His(p.R1349H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48734627:48734627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.438G>T
AA Mutation	p.Glu146Asp(p.E146D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48632359:48632359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4444G>T
AA Mutation	p.Gly1482Cys(p.G1482C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48627920:48627920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4810C>T
AA Mutation	p.Arg1604Trp(p.R1604W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48649543:48649543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3062G>A
AA Mutation	p.Cys1021Tyr(p.C1021Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48726375:48726375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.536G>A
AA Mutation	p.Gly179Glu(p.G179E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48651416:48651416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2635T>C
AA Mutation	p.Cys879Arg(p.C879R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000371941
Start	48747880:48747880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.220G>A
AA Mutation	p.Ala74Thr(p.A74T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48649570:48649570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3035T>G
AA Mutation	p.Leu1012Arg(p.L1012R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48653372:48653372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749750409
CDS Mutation	c.2335G>A
AA Mutation	p.Glu779Lys(p.E779K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48726370:48726370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148948169
CDS Mutation	c.541C>T
AA Mutation	p.Arg181Trp(p.R181W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48652644:48652644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2409G>T
AA Mutation	p.Glu803Asp(p.E803D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48655308:48655308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139250516
CDS Mutation	c.2191G>A
AA Mutation	p.Val731Ile(p.V731I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48645879:48645879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747490930
CDS Mutation	c.3484G>A
AA Mutation	p.Asp1162Asn(p.D1162N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48708400:48708400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776160255
CDS Mutation	c.643G>A
AA Mutation	p.Gly215Ser(p.G215S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000371941
Start	48650895:48650895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2816A>T
AA Mutation	p.Glu939Val(p.E939V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48646025:48646025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3338G>A
AA Mutation	p.Gly1113Asp(p.G1113D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48650178:48650178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2846G>A
AA Mutation	p.Ser949Asn(p.S949N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48651031:48651031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2680G>T
AA Mutation	p.Asp894Tyr(p.D894Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48660005:48660005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1795G>A
AA Mutation	p.Glu599Lys(p.E599K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48639865:48639865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3805C>T
AA Mutation	p.Arg1269Cys(p.R1269C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371941
Start	48651020:48651020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763619070
CDS Mutation	c.2691C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371941
Start	48642466:48642466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3625C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371941
Start	48632318:48632318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768896615
CDS Mutation	c.4485G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371941
Start	48629508:48629508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200783880
CDS Mutation	c.4707G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371941
Start	48827702:48827702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371941
Start	48650141:48650141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368665525
CDS Mutation	c.2883G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371941
Start	48651408:48651408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2643C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371941
Start	48650154:48650155(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2869dupC
AA Mutation	p.Leu957ProfsTer50(p.L957Pfs*50)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PREX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48644433:48644433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3577T>A
AA Mutation	p.Leu1193Met(p.L1193M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48625904:48625904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4961C>T
AA Mutation	p.Pro1654Leu(p.P1654L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48650926:48650926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2785A>C
AA Mutation	p.Ser929Arg(p.S929R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48651424:48651424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2627C>G
AA Mutation	p.Pro876Arg(p.P876R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48650004:48650004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763984566
CDS Mutation	c.3020C>T
AA Mutation	p.Pro1007Leu(p.P1007L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48642207:48642207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747211086
CDS Mutation	c.3736G>A
AA Mutation	p.Glu1246Lys(p.E1246K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48649459:48649459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3146G>C
AA Mutation	p.Ser1049Thr(p.S1049T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48645929:48645929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3434A>C
AA Mutation	p.Lys1145Thr(p.K1145T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371941
Start	48650098:48650098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2926C>G
AA Mutation	p.Leu976Val(p.L976V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371941
Start	48651420:48651420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143006779
CDS Mutation	c.2631C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371941
Start	48650141:48650141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368665525
CDS Mutation	c.2883G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371941
Start	48632318:48632318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768896615
CDS Mutation	c.4485G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371941
Start	48632500:48632500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774259011
CDS Mutation	c.4407G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371941
Start	48659970:48659970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1830G>A
Mutation Classification	Silent
Feature Type	Transcript