Colon Cancer: Gene >> CPPED1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381774
Start	12781208:12781208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.266G>A
AA Mutation	p.Gly89Asp(p.G89D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381774
Start	12781277:12781277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367880734
CDS Mutation	c.197G>A
AA Mutation	p.Arg66His(p.R66H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381774
Start	12664978:12664978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369945677
CDS Mutation	c.853G>A
AA Mutation	p.Ala285Thr(p.A285T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381774
Start	12704859:12704859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764348357
CDS Mutation	c.480C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381774
Start	12704628:12704628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764518637
CDS Mutation	c.711C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381774
Start	12781261:12781261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776501530
CDS Mutation	c.213C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381774
Start	12781393:12781393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566259758
CDS Mutation	c.81C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381774
Start	12704697:12704697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200745290
CDS Mutation	c.642C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381774
Start	12803733:12803733(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs759977975
CDS Mutation	c.44delG
AA Mutation	p.Gly15AlafsTer31(p.G15Afs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CPPED1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381774
Start	12704687:12704687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771021460
CDS Mutation	c.652G>A
AA Mutation	p.Asp218Asn(p.D218N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381774
Start	12704867:12704867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145004672
CDS Mutation	c.472G>A
AA Mutation	p.Val158Ile(p.V158I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381774
Start	12704838:12704838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.501C>A
AA Mutation	p.Phe167Leu(p.F167L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381774
Start	12781310:12781310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539774293
CDS Mutation	c.164A>G
AA Mutation	p.Asp55Gly(p.D55G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381774
Start	12665054:12665054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.777C>T
Mutation Classification	Silent
Feature Type	Transcript