Colon Cancer: Gene >> CYP1A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379727
Start	74722864:74722864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.234T>G
AA Mutation	p.Ile78Met(p.I78M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379727
Start	74721221:74721221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201651069
CDS Mutation	c.1144G>A
AA Mutation	p.Val382Ile(p.V382I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379727
Start	74720496:74720496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56343424
CDS Mutation	c.1532G>A
AA Mutation	p.Arg511His(p.R511H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379727
Start	74722984:74722984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.114G>T
AA Mutation	p.Lys38Asn(p.K38N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379727
Start	74722947:74722947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.151C>T
AA Mutation	p.His51Tyr(p.H51Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379727
Start	74722881:74722881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373568981
CDS Mutation	c.217G>A
AA Mutation	p.Val73Met(p.V73M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379727
Start	74722697:74722697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367709511
CDS Mutation	c.401G>A
AA Mutation	p.Arg134His(p.R134H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379727
Start	74720653:74720653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371662141
CDS Mutation	c.1375G>A
AA Mutation	p.Gly459Ser(p.G459S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379727
Start	74722798:74722798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377233098
CDS Mutation	c.300C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379727
Start	74721002:74721002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1218T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CYP1A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379727
Start	74722359:74722359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.739T>C
AA Mutation	p.Ser247Pro(p.S247P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379727
Start	74722444:74722444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000379727
Start	74721423:74721423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539280298
CDS Mutation	c.1033G>T
AA Mutation	p.Glu345Ter(p.E345*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript