Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CYP2C9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260682
Start	94941894:94941894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.205T>G
AA Mutation	p.Phe69Val(p.F69V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260682
Start	94949158:94949158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.693C>A
AA Mutation	p.Asn231Lys(p.N231K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260682
Start	94938759:94938759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.77G>T
AA Mutation	p.Arg26Ile(p.R26I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260682
Start	94986047:94986047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1164A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260682
Start	94941929:94941929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200794294
CDS Mutation	c.240T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CYP2C9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260682
Start	94947894:94947894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.597A>C
AA Mutation	p.Glu199Asp(p.E199D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260682
Start	94981242:94981242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1021G>T
AA Mutation	p.Asp341Tyr(p.D341Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260682
Start	94947851:94947851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.554A>C
AA Mutation	p.Lys185Thr(p.K185T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260682
Start	94988852:94988852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776908257
CDS Mutation	c.1297C>T
AA Mutation	p.Arg433Trp(p.R433W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260682
Start	94988917:94988917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1362G>T
AA Mutation	p.Gln454His(p.Q454H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript