Colon Cancer: Gene >> CEP72

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264935
Start	637807:637807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750420955
CDS Mutation	c.1195G>A
AA Mutation	p.Asp399Asn(p.D399N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264935
Start	644405:644405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577972731
CDS Mutation	c.1646C>T
AA Mutation	p.Thr549Met(p.T549M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264935
Start	637565:637565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.953C>T
AA Mutation	p.Ser318Leu(p.S318L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264935
Start	633920:633920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767316211
CDS Mutation	c.664C>T
AA Mutation	p.Arg222Cys(p.R222C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264935
Start	653007:653007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1798G>A
AA Mutation	p.Glu600Lys(p.E600K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264935
Start	640480:640480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1415A>G
AA Mutation	p.Glu472Gly(p.E472G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264935
Start	639131:639131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1249G>A
AA Mutation	p.Ala417Thr(p.A417T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264935
Start	647835:647835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1697G>A
AA Mutation	p.Gly566Asp(p.G566D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264935
Start	647893:647893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142569661
CDS Mutation	c.1755G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264935
Start	633778:633778(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.525delC
AA Mutation	p.Arg176GlufsTer23(p.R176Efs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CEP72

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264935
Start	644364:644364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1605G>T
AA Mutation	p.Leu535Phe(p.L535F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264935
Start	644337:644337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1578G>T
AA Mutation	p.Glu526Asp(p.E526D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264935
Start	647836:647836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1698C>T
Mutation Classification	Silent
Feature Type	Transcript