Colon Cancer: Gene >> CYP2F1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331105
Start	41121538:41121538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565G>A
AA Mutation	p.Asp189Asn(p.D189N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331105
Start	41116349:41116349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161C>A
AA Mutation	p.Ser54Tyr(p.S54Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331105
Start	41122008:41122008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763970224
CDS Mutation	c.697C>T
AA Mutation	p.Arg233Cys(p.R233C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331105
Start	41124857:41124857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371341517
CDS Mutation	c.1103C>T
AA Mutation	p.Pro368Leu(p.P368L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331105
Start	41121517:41121517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544G>A
AA Mutation	p.Val182Met(p.V182M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331105
Start	41122047:41122047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370865507
CDS Mutation	c.736G>A
AA Mutation	p.Ala246Thr(p.A246T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331105
Start	41125523:41125523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768113626
CDS Mutation	c.1183G>A
AA Mutation	p.Val395Ile(p.V395I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331105
Start	41122056:41122056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770227087
CDS Mutation	c.745G>A
AA Mutation	p.Val249Ile(p.V249I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000331105
Start	41120370:41120370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358C>T
AA Mutation	p.Arg120Ter(p.R120*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CYP2F1

No Mutation Annotation!