Colon Cancer: Gene >> DCLRE1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369563
Start	113911524:113911524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.932G>A
AA Mutation	p.Ser311Asn(p.S311N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369563
Start	113908162:113908162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774706467
CDS Mutation	c.509G>A
AA Mutation	p.Arg170Gln(p.R170Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369563
Start	113905660:113905660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.74G>A
AA Mutation	p.Arg25His(p.R25H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369563
Start	113912118:113912118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1526T>C
AA Mutation	p.Val509Ala(p.V509A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369563
Start	113912123:113912123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1531T>A
AA Mutation	p.Phe511Ile(p.F511I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369563
Start	113911848:113911848(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1259delA
AA Mutation	p.Lys420ArgfsTer3(p.K420Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DCLRE1B

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369563
Start	113907127:113907127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.321C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369563
Start	113907091:113907091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547539348
CDS Mutation	c.285C>T
Mutation Classification	Silent
Feature Type	Transcript