Colon Cancer: Gene >> CYP3A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336411
Start	99770171:99770171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383G>T
AA Mutation	p.Arg128Ile(p.R128I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336411
Start	99766405:99766405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.837G>T
AA Mutation	p.Gln279His(p.Q279H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336411
Start	99768480:99768480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.544G>T
AA Mutation	p.Asp182Tyr(p.D182Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336411
Start	99762124:99762124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1170A>C
AA Mutation	p.Lys390Asn(p.K390N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336411
Start	99784041:99784041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.41T>G
AA Mutation	p.Leu14Arg(p.L14R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336411
Start	99762185:99762185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1109C>T
AA Mutation	p.Ala370Val(p.A370V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000336411
Start	99778030:99778030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.216G>T
AA Mutation	p.Trp72Cys(p.W72C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CYP3A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336411
Start	99766413:99766413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.829G>T
AA Mutation	p.Asp277Tyr(p.D277Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336411
Start	99762156:99762156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138G>T
AA Mutation	p.Asp380Tyr(p.D380Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript