Colon Cancer: Gene >> CYP3A7

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000336374
Start	99715905:99715905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146249663
CDS Mutation	c.523G>A
AA Mutation	p.Val175Ile(p.V175I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336374
Start	99710826:99710826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.932G>T
AA Mutation	p.Ser311Ile(p.S311I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336374
Start	99735038:99735038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.56T>C
AA Mutation	p.Leu19Pro(p.L19P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336374
Start	99731064:99731064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760875340
CDS Mutation	c.160C>T
AA Mutation	p.Arg54Cys(p.R54C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336374
Start	99715776:99715776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652C>T
AA Mutation	p.Pro218Ser(p.P218S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336374
Start	99714575:99714575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371807974
CDS Mutation	c.778C>T
AA Mutation	p.Arg260Cys(p.R260C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336374
Start	99722301:99722301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336374
Start	99720331:99720331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767410266
CDS Mutation	c.300T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336374
Start	99710768:99710768(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.990delA
AA Mutation	p.Val331CysfsTer30(p.V331Cfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000336374
Start	99720342:99720342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289G>T
AA Mutation	p.Glu97Ter(p.E97*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000336374
Start	99722327:99722327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187G>T
AA Mutation	p.Glu63Ter(p.E63*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000336374
Start	99710764:99710764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.994C>T
AA Mutation	p.Gln332Ter(p.Q332*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CYP3A7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336374
Start	99731127:99731127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.97T>G
AA Mutation	p.Phe33Val(p.F33V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336374
Start	99722301:99722301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213C>A
Mutation Classification	Silent
Feature Type	Transcript