Colon Cancer: Gene >> PEPD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244137
Start	33413605:33413605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577079343
CDS Mutation	c.710G>A
AA Mutation	p.Arg237His(p.R237H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000244137
Start	33387417:33387417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765552774
CDS Mutation	c.1409G>A
AA Mutation	p.Arg470His(p.R470H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000244137
Start	33478053:33478053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372629704
CDS Mutation	c.541G>A
AA Mutation	p.Val181Ile(p.V181I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000244137
Start	33387904:33387904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1330C>T
AA Mutation	p.Arg444Cys(p.R444C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000244137
Start	33387390:33387390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1436T>C
AA Mutation	p.Met479Thr(p.M479T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000244137
Start	33401756:33401756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1063319
CDS Mutation	c.932G>A
AA Mutation	p.Arg311Gln(p.R311Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244137
Start	33511111:33511111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.246C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244137
Start	33413604:33413604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PEPD

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244137
Start	33478087:33478087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377714630
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244137
Start	33401863:33401863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript