Colon Cancer: Gene >> PARP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250416
Start	20354874:20354874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140156644
CDS Mutation	c.868C>T
AA Mutation	p.Arg290Trp(p.R290W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250416
Start	20357757:20357757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1712A>G
AA Mutation	p.Tyr571Cys(p.Y571C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250416
Start	20345036:20345036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.151C>T
AA Mutation	p.Pro51Ser(p.P51S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000250416
Start	20352339:20352339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631A>G
AA Mutation	p.Asn211Asp(p.N211D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000250416
Start	20355898:20355898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746484531
CDS Mutation	c.1007C>T
AA Mutation	p.Ala336Val(p.A336V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000250416
Start	20357753:20357753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761738969
CDS Mutation	c.1708C>T
AA Mutation	p.Arg570Trp(p.R570W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000250416
Start	20343682:20343682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.41C>T
AA Mutation	p.Ala14Val(p.A14V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PARP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250416
Start	20356376:20356376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1210T>G
AA Mutation	p.Leu404Val(p.L404V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250416
Start	20351111:20351111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.525C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250416
Start	20352260:20352260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770825459
CDS Mutation	c.552G>A
Mutation Classification	Silent
Feature Type	Transcript