Colon Cancer: Gene >> DPEP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268793
Start	67977807:67977807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201970507
CDS Mutation	c.854G>A
AA Mutation	p.Arg285His(p.R285H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268793
Start	67980216:67980216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.240C>G
AA Mutation	p.Phe80Leu(p.F80L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268793
Start	67980238:67980238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.218C>T
AA Mutation	p.Thr73Met(p.T73M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268793
Start	67980421:67980421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.35G>A
AA Mutation	p.Arg12His(p.R12H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268793
Start	67980130:67980130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150317704
CDS Mutation	c.326C>T
AA Mutation	p.Ala109Val(p.A109V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268793
Start	67978557:67978557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559G>T
AA Mutation	p.Asp187Tyr(p.D187Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268793
Start	67980249:67980249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.207A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268793
Start	67977310:67977310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1053G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268793
Start	67975969:67975969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1338G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268793
Start	67976186:67976186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1212G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000268793
Start	67977652:67977652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1008+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DPEP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268793
Start	67980194:67980194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262G>A
AA Mutation	p.Ala88Thr(p.A88T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268793
Start	67978544:67978544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757782418
CDS Mutation	c.572G>A
AA Mutation	p.Arg191His(p.R191H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript