Colon Cancer: Gene >> CYP2B6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324071
Start	41012432:41012432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1099G>A
AA Mutation	p.Val367Met(p.V367M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324071
Start	40991379:40991379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.74A>G
AA Mutation	p.Asn25Ser(p.N25S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324071
Start	41010046:41010046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138594605
CDS Mutation	c.875C>T
AA Mutation	p.Thr292Met(p.T292M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324071
Start	40991409:40991409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781365650
CDS Mutation	c.104G>A
AA Mutation	p.Arg35His(p.R35H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324071
Start	41010098:41010098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768992518
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324071
Start	41016752:41016752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745638870
CDS Mutation	c.1401C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324071
Start	41016683:41016683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775699069
CDS Mutation	c.1332G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324071
Start	41004126:41004126(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.301delA
AA Mutation	p.Ile101SerfsTer13(p.I101Sfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CYP2B6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324071
Start	40991453:40991453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.148G>T
AA Mutation	p.Gly50Cys(p.G50C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324071
Start	40991471:40991471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166C>T
Mutation Classification	Silent
Feature Type	Transcript