Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TPO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1433482:1433482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224C>A
AA Mutation	p.Ser75Tyr(p.S75Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1436255:1436255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755626297
CDS Mutation	c.353C>T
AA Mutation	p.Ala118Val(p.A118V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1496708:1496708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745501383
CDS Mutation	c.2329C>T
AA Mutation	p.Arg777Trp(p.R777W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1487895:1487895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575622093
CDS Mutation	c.1672G>A
AA Mutation	p.Glu558Lys(p.E558K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1540697:1540697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753786141
CDS Mutation	c.2722C>T
AA Mutation	p.Arg908Trp(p.R908W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1477251:1477251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.985G>A
AA Mutation	p.Val329Met(p.V329M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1504037:1504037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781420871
CDS Mutation	c.2476G>A
AA Mutation	p.Ala826Thr(p.A826T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000329066
Start	1540721:1540721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2746C>A
AA Mutation	p.Gln916Lys(p.Q916K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1414421:1414421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369441749
CDS Mutation	c.13G>A
AA Mutation	p.Ala5Thr(p.A5T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1477288:1477288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774989776
CDS Mutation	c.1022G>A
AA Mutation	p.Arg341Gln(p.R341Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1487905:1487905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200475577
CDS Mutation	c.1682C>T
AA Mutation	p.Thr561Met(p.T561M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1496664:1496664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139734552
CDS Mutation	c.2285G>A
AA Mutation	p.Arg762His(p.R762H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1423120:1423120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.170C>T
AA Mutation	p.Thr57Met(p.T57M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1456187:1456187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780371451
CDS Mutation	c.724G>A
AA Mutation	p.Ala242Thr(p.A242T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1540679:1540679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368181428
CDS Mutation	c.2704G>A
AA Mutation	p.Val902Ile(p.V902I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1456223:1456223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371917329
CDS Mutation	c.760G>A
AA Mutation	p.Gly254Arg(p.G254R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1423058:1423058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.108G>T
AA Mutation	p.Glu36Asp(p.E36D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000329066
Start	1496597:1496597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762116311
CDS Mutation	c.2218G>A
AA Mutation	p.Asp740Asn(p.D740N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1516922:1516922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373501176
CDS Mutation	c.2558C>T
AA Mutation	p.Ser853Leu(p.S853L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1493888:1493888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1855G>A
AA Mutation	p.Ala619Thr(p.A619T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000329066
Start	1453822:1453822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746942915
CDS Mutation	c.611C>T
AA Mutation	p.Pro204Leu(p.P204L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329066
Start	1493827:1493827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141377851
CDS Mutation	c.1794C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329066
Start	1484700:1484700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377537666
CDS Mutation	c.1443G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329066
Start	1453790:1453790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.579C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329066
Start	1453805:1453805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375152400
CDS Mutation	c.594C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329066
Start	1423115:1423115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149346954
CDS Mutation	c.165C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329066
Start	1516887:1516887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367751257
CDS Mutation	c.2523C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329066
Start	1477241:1477241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.975C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329066
Start	1540693:1540693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149611408
CDS Mutation	c.2718G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329066
Start	1477148:1477148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.882C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329066
Start	1456184:1456185(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.721_722insC
AA Mutation	p.Ile241ThrfsTer18(p.I241Tfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TPO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1493884:1493884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1851C>A
AA Mutation	p.Ser617Arg(p.S617R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1423107:1423107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199694732
CDS Mutation	c.157G>A
AA Mutation	p.Ala53Thr(p.A53T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1503967:1503967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2406C>A
AA Mutation	p.Asp802Glu(p.D802E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1487838:1487838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1615A>T
AA Mutation	p.Ile539Leu(p.I539L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1496028:1496028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2046G>T
AA Mutation	p.Gln682His(p.Q682H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000329066
Start	1493828:1493828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757274238
CDS Mutation	c.1795G>A
AA Mutation	p.Gly599Ser(p.G599S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329066
Start	1504060:1504060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142148533
CDS Mutation	c.2499C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329066
Start	1456174:1456174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756113203
CDS Mutation	c.711C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329066
Start	1503975:1503976(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs775551134
CDS Mutation	c.2421dupC
AA Mutation	p.Cys808LeufsTer72(p.C808Lfs*72)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript