Colon Cancer: Gene >> CYP2C19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371321
Start	94842870:94842870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995G>A
AA Mutation	p.Gly332Asp(p.G332D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371321
Start	94852738:94852738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56337013
CDS Mutation	c.1297C>T
AA Mutation	p.Arg433Trp(p.R433W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371321
Start	94820550:94820550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.874G>C
AA Mutation	p.Ala292Pro(p.A292P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371321
Start	94852803:94852803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1362G>T
AA Mutation	p.Gln454His(p.Q454H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371321
Start	94775188:94775188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.299T>G
AA Mutation	p.Phe100Cys(p.F100C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371321
Start	94842959:94842959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1084A>G
AA Mutation	p.Ile362Val(p.I362V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371321
Start	94852836:94852836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1395G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000371321
Start	94762875:94762875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.168+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CYP2C19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371321
Start	94852820:94852820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1379C>A
AA Mutation	p.Ser460Tyr(p.S460Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript