Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> BCOR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40052336:40052336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768919602
CDS Mutation	c.5041C>T
AA Mutation	p.Arg1681Cys(p.R1681C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40063721:40063721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3734C>T
AA Mutation	p.Ala1245Val(p.A1245V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40073497:40073497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143744110
CDS Mutation	c.1849G>A
AA Mutation	p.Ala617Thr(p.A617T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40053889:40053889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759505174
CDS Mutation	c.4973A>G
AA Mutation	p.Gln1658Arg(p.Q1658R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40073942:40073942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1404C>A
AA Mutation	p.His468Gln(p.H468Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40064389:40064389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373730020
CDS Mutation	c.3449A>G
AA Mutation	p.Glu1150Gly(p.E1150G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40073819:40073819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1527G>T
AA Mutation	p.Trp509Cys(p.W509C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40074439:40074439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.907G>A
AA Mutation	p.Ala303Thr(p.A303T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40053997:40053997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4865G>T
AA Mutation	p.Gly1622Val(p.G1622V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40074250:40074250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1096A>G
AA Mutation	p.Thr366Ala(p.T366A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40062796:40062796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4123C>T
AA Mutation	p.Arg1375Trp(p.R1375W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40074618:40074618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.728G>A
AA Mutation	p.Arg243His(p.R243H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40073016:40073016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2330C>G
AA Mutation	p.Pro777Arg(p.P777R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40073638:40073638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748813798
CDS Mutation	c.1708G>A
AA Mutation	p.Ala570Thr(p.A570T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40064507:40064507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371897880
CDS Mutation	c.3331C>T
AA Mutation	p.Pro1111Ser(p.P1111S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40074931:40074931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415G>A
AA Mutation	p.Gly139Arg(p.G139R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378444
Start	40073147:40073147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140693978
CDS Mutation	c.2199G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378444
Start	40072619:40072619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2727C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378444
Start	40052187:40052187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375139386
CDS Mutation	c.5190G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378444
Start	40052337:40052337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5040T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378444
Start	40075118:40075118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378444
Start	40057226:40057226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4524C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378444
Start	40053926:40053926(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4936delC
AA Mutation	p.Leu1646SerfsTer28(p.L1646Sfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378444
Start	40071029:40071029(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3182delA
AA Mutation	p.Lys1061SerfsTer52(p.K1061Sfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378444
Start	40054000:40054000(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs797044647
CDS Mutation	c.4862delC
AA Mutation	p.Pro1621GlnfsTer53(p.P1621Qfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378444
Start	40074969:40074969(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.377delC
AA Mutation	p.Pro126ArgfsTer35(p.P126Rfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378444
Start	40072832:40072832(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2514delC
AA Mutation	p.Lys839SerfsTer17(p.K839Sfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378444
Start	40077857:40077857(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.73delG
AA Mutation	p.Ala25ArgfsTer9(p.A25Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378444
Start	40073760:40073760(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1586delA
AA Mutation	p.Asn529ThrfsTer60(p.N529Tfs*60)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000378444
Start	40074322:40074322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024C>T
AA Mutation	p.Arg342Ter(p.R342*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000378444
Start	40055470:40055470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4639C>T
AA Mutation	p.Arg1547Ter(p.R1547*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000378444
Start	40063731:40063731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3724C>T
AA Mutation	p.Gln1242Ter(p.Q1242*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000378444
Start	40057210:40057210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4540C>T
AA Mutation	p.Arg1514Ter(p.R1514*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	stop_gained
Transcription ID	ENST00000378444
Start	40063806:40063806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3649C>T
AA Mutation	p.Arg1217Ter(p.R1217*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000378444
Start	40074412:40074412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934C>T
AA Mutation	p.Gln312Ter(p.Q312*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378444
Start	40063811:40063812(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3643dupA
AA Mutation	p.Arg1215LysfsTer30(p.R1215Kfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378444
Start	40072831:40072832(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2514dupC
AA Mutation	p.Lys839GlnfsTer5(p.K839Qfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378444
Start	40073886:40073887(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1456_1459dupACAC
AA Mutation	p.Leu487HisfsTer13(p.L487Hfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BCOR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40073674:40073674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1672T>G
AA Mutation	p.Ser558Ala(p.S558A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40055375:40055375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4734C>A
AA Mutation	p.Phe1578Leu(p.F1578L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378444
Start	40054328:40054328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4747T>G
AA Mutation	p.Leu1583Val(p.L1583V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378444
Start	40072956:40072957(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2389_2390delGT
AA Mutation	p.Val797CysfsTer19(p.V797Cfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript