Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CENPJ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24905733:24905733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2305A>C
AA Mutation	p.Ile769Leu(p.I769L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24912750:24912750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.276A>C
AA Mutation	p.Lys92Asn(p.K92N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24912892:24912892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377249179
CDS Mutation	c.134G>A
AA Mutation	p.Arg45Gln(p.R45Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24884421:24884421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3520C>T
AA Mutation	p.Pro1174Ser(p.P1174S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24906905:24906905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761545596
CDS Mutation	c.1133G>A
AA Mutation	p.Arg378Gln(p.R378Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24884346:24884346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3595C>G
AA Mutation	p.Gln1199Glu(p.Q1199E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24908097:24908097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895A>G
AA Mutation	p.Thr299Ala(p.T299A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24883192:24883192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4002G>T
AA Mutation	p.Met1334Ile(p.M1334I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24889394:24889394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3223T>C
AA Mutation	p.Ser1075Pro(p.S1075P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24907142:24907142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1026A>T
AA Mutation	p.Leu342Phe(p.L342F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24906105:24906105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541232925
CDS Mutation	c.1933C>T
AA Mutation	p.Arg645Cys(p.R645C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24906078:24906078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140927921
CDS Mutation	c.1960G>A
AA Mutation	p.Ala654Thr(p.A654T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24883307:24883307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3887A>C
AA Mutation	p.Lys1296Thr(p.K1296T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24909949:24909949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706A>G
AA Mutation	p.Ile236Val(p.I236V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24884060:24884060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3727A>C
AA Mutation	p.Lys1243Gln(p.K1243Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24912701:24912701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325G>A
AA Mutation	p.Ala109Thr(p.A109T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24906636:24906636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1402C>A
AA Mutation	p.Leu468Ile(p.L468I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24884050:24884050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767833776
CDS Mutation	c.3737C>T
AA Mutation	p.Thr1246Met(p.T1246M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381884
Start	24906820:24906820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1218T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381884
Start	24905743:24905743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747058868
CDS Mutation	c.2295C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381884
Start	24906934:24906934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1104A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381884
Start	24906256:24906256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1782C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381884
Start	24906628:24906628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115628561
CDS Mutation	c.1410G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381884
Start	24904034:24904034(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2717delT
AA Mutation	p.Leu906Ter(p.L906*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000381884
Start	24884409:24884409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760698184
CDS Mutation	c.3532C>T
AA Mutation	p.Arg1178Ter(p.R1178*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000381884
Start	24889388:24889388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763373509
CDS Mutation	c.3229C>T
AA Mutation	p.Arg1077Ter(p.R1077*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381884
Start	24907099:24907100(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1068dupA
AA Mutation	p.Gln357ThrfsTer28(p.Q357Tfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000381884
Start	24903924:24903924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2825+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CENPJ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24909949:24909949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706A>G
AA Mutation	p.Ile236Val(p.I236V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24906848:24906848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1190A>T
AA Mutation	p.Glu397Val(p.E397V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24906231:24906231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1807A>G
AA Mutation	p.Arg603Gly(p.R603G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24899456:24899456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2954G>T
AA Mutation	p.Arg985Ile(p.R985I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381884
Start	24906268:24906268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1770T>G
AA Mutation	p.Phe590Leu(p.F590L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381884
Start	24899566:24899566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2844C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381884
Start	24883197:24883197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3997C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381884
Start	24899542:24899542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2868A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000381884
Start	24883251:24883251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3943G>T
AA Mutation	p.Glu1315Ter(p.E1315*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000381884
Start	24906537:24906537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1501G>T
AA Mutation	p.Glu501Ter(p.E501*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000381884
Start	24911945:24911945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.568+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript