Colon Cancer: Gene >> CYP26A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93074953:93074953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589G>A
AA Mutation	p.Glu197Lys(p.E197K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93075875:93075875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142962735
CDS Mutation	c.914C>T
AA Mutation	p.Thr305Met(p.T305M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93075847:93075847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.886G>A
AA Mutation	p.Glu296Lys(p.E296K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93074371:93074371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253G>A
AA Mutation	p.Gly85Arg(p.G85R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93076610:93076610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1066A>C
AA Mutation	p.Ile356Leu(p.I356L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93074360:93074360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.242C>T
AA Mutation	p.Thr81Met(p.T81M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93075028:93075028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.664T>G
AA Mutation	p.Phe222Val(p.F222V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93075868:93075868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907G>A
AA Mutation	p.Glu303Lys(p.E303K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93074341:93074341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.223T>C
AA Mutation	p.Tyr75His(p.Y75H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000224356
Start	93077199:93077199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1389T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000224356
Start	93075903:93075903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000224356
Start	93075169:93075169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.726C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000224356
Start	93074802:93074802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544822437
CDS Mutation	c.438C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000224356
Start	93075277:93075277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779220881
CDS Mutation	c.834G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CYP26A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93076629:93076629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1085A>T
AA Mutation	p.Glu362Val(p.E362V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93075860:93075860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899G>A
AA Mutation	p.Gly300Glu(p.G300E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000224356
Start	93077301:93077301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1491C>A
Mutation Classification	Silent
Feature Type	Transcript