Colon Cancer: Gene >> PNKP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322344
Start	49864192:49864192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.623C>T
AA Mutation	p.Ala208Val(p.A208V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322344
Start	49861639:49861639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1355C>T
AA Mutation	p.Ala452Val(p.A452V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322344
Start	49861788:49861788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282G>A
AA Mutation	p.Ala428Thr(p.A428T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322344
Start	49862410:49862410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368069267
CDS Mutation	c.990G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322344
Start	49862724:49862724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148491228
CDS Mutation	c.831G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PNKP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322344
Start	49862578:49862578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.896C>T
AA Mutation	p.Pro299Leu(p.P299L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322344
Start	49861496:49861496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374547164
CDS Mutation	c.1401G>A
Mutation Classification	Silent
Feature Type	Transcript