Colon Cancer: Gene >> PARP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24435155:24435155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140886733
CDS Mutation	c.3986C>T
AA Mutation	p.Pro1329Leu(p.P1329L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24441963:24441963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3549G>T
AA Mutation	p.Glu1183Asp(p.E1183D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24442633:24442633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3500C>A
AA Mutation	p.Ser1167Tyr(p.S1167Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24501697:24501697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270G>T
AA Mutation	p.Lys90Asn(p.K90N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24469952:24469952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1988A>G
AA Mutation	p.Asp663Gly(p.D663G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24452515:24452515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2905T>C
AA Mutation	p.Ser969Pro(p.S969P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24435210:24435210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3931T>C
AA Mutation	p.Ser1311Pro(p.S1311P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24503712:24503712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.65A>G
AA Mutation	p.Gln22Arg(p.Q22R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24486237:24486237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1283G>T
AA Mutation	p.Ser428Ile(p.S428I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24469944:24469944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1996G>T
AA Mutation	p.Ala666Ser(p.A666S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24455130:24455130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2645A>G
AA Mutation	p.Asp882Gly(p.D882G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24441857:24441857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368137267
CDS Mutation	c.3655G>A
AA Mutation	p.Val1219Ile(p.V1219I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24449732:24449732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3100A>G
AA Mutation	p.Ser1034Gly(p.S1034G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24459105:24459105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2363C>A
AA Mutation	p.Ser788Tyr(p.S788Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24498180:24498180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372500814
CDS Mutation	c.527C>T
AA Mutation	p.Ser176Leu(p.S176L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24501644:24501644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323C>T
AA Mutation	p.Ala108Val(p.A108V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381989
Start	24434623:24434623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4518C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381989
Start	24456344:24456344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771263287
CDS Mutation	c.2559C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381989
Start	24460023:24460023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34385526
CDS Mutation	c.2247C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381989
Start	24431471:24431471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4752C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000381989
Start	24494724:24494724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.592-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PARP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24501642:24501642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325A>C
AA Mutation	p.Ser109Arg(p.S109R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381989
Start	24492582:24492582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.892G>A
AA Mutation	p.Glu298Lys(p.E298K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000381989
Start	24449815:24449815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3017C>A
AA Mutation	p.Ser1006Tyr(p.S1006Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381989
Start	24486185:24486185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765885299
CDS Mutation	c.1335C>T
Mutation Classification	Silent
Feature Type	Transcript