Colon Cancer: Gene >> CYP26B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000001146
Start	72132486:72132486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1280G>A
AA Mutation	p.Gly427Asp(p.G427D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000001146
Start	72134882:72134882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.740T>C
AA Mutation	p.Leu247Pro(p.L247P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000001146
Start	72147785:72147785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.50C>T
AA Mutation	p.Ala17Val(p.A17V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000001146
Start	72135320:72135320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201533354
CDS Mutation	c.529G>A
AA Mutation	p.Glu177Lys(p.E177K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000001146
Start	72144192:72144192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.226C>T
AA Mutation	p.Arg76Trp(p.R76W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000001146
Start	72133138:72133138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772338043
CDS Mutation	c.1031G>A
AA Mutation	p.Arg344His(p.R344H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000001146
Start	72143997:72143997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.421A>G
AA Mutation	p.Lys141Glu(p.K141E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000001146
Start	72133190:72133190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199909218
CDS Mutation	c.979C>T
AA Mutation	p.Arg327Trp(p.R327W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000001146
Start	72135341:72135341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.508C>T
AA Mutation	p.Arg170Cys(p.R170C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000001146
Start	72144075:72144075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.343A>G
AA Mutation	p.Thr115Ala(p.T115A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000001146
Start	72133079:72133079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090C>A
AA Mutation	p.Leu364Met(p.L364M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000001146
Start	72144153:72144153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.265T>G
AA Mutation	p.Leu89Val(p.L89V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000001146
Start	72135339:72135339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145145054
CDS Mutation	c.510C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000001146
Start	72144100:72144100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CYP26B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000001146
Start	72133189:72133189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200922951
CDS Mutation	c.980G>A
AA Mutation	p.Arg327Gln(p.R327Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000001146
Start	72134863:72134863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.759G>T
AA Mutation	p.Glu253Asp(p.E253D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000001146
Start	72147741:72147741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000001146
Start	72132368:72132368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1398G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000001146
Start	72144103:72144103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.315C>A
Mutation Classification	Silent
Feature Type	Transcript