Colon Cancer: Gene >> CYP3A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222982
Start	99664027:99664027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.739A>C
AA Mutation	p.Asn247His(p.N247H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222982
Start	99666962:99666962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.422A>C
AA Mutation	p.Lys141Thr(p.K141T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222982
Start	99664024:99664024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.742T>G
AA Mutation	p.Phe248Val(p.F248V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222982
Start	99650173:99650173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1313C>A
AA Mutation	p.Pro438His(p.P438H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222982
Start	99665300:99665300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.536A>G
AA Mutation	p.Tyr179Cys(p.Y179C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222982
Start	99666639:99666639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000222982
Start	99674586:99674586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CYP3A5

No Mutation Annotation!