Colon Cancer: Gene >> DECR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220764
Start	90001545:90001545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781613500
CDS Mutation	c.53G>T
AA Mutation	p.Gly18Val(p.G18V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220764
Start	90017259:90017259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.205A>G
AA Mutation	p.Thr69Ala(p.T69A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220764
Start	90044886:90044886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776A>C
AA Mutation	p.Glu259Ala(p.E259A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220764
Start	90020961:90020961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470C>T
AA Mutation	p.Ser157Phe(p.S157F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220764
Start	90018933:90018933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763777845
CDS Mutation	c.297C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220764
Start	90042791:90042791(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.733delA
AA Mutation	p.Thr245ProfsTer18(p.T245Pfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DECR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220764
Start	90051735:90051735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.944G>T
AA Mutation	p.Arg315Ile(p.R315I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000220764
Start	90036843:90036843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568G>A
AA Mutation	p.Ala190Thr(p.A190T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript