Colon Cancer: Gene >> CYP1B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000610745
Start	38074620:38074620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769699570
CDS Mutation	c.769G>A
AA Mutation	p.Val257Ile(p.V257I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000610745
Start	38071212:38071212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1142T>C
AA Mutation	p.Val381Ala(p.V381A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000610745
Start	38070949:38070949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28936701
CDS Mutation	c.1405C>T
AA Mutation	p.Arg469Trp(p.R469W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000610745
Start	38074932:38074932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368041729
CDS Mutation	c.457C>T
AA Mutation	p.Arg153Cys(p.R153C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000610745
Start	38071185:38071185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56010818
CDS Mutation	c.1169G>A
AA Mutation	p.Arg390His(p.R390H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000610745
Start	38074740:38074740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649G>A
AA Mutation	p.Asp217Asn(p.D217N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000610745
Start	38074613:38074613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776G>A
AA Mutation	p.Arg259His(p.R259H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000610745
Start	38070937:38070937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138388190
CDS Mutation	c.1417G>A
AA Mutation	p.Glu473Lys(p.E473K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000610745
Start	38075077:38075077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.312C>A
AA Mutation	p.His104Gln(p.H104Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610745
Start	38074696:38074696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610745
Start	38074678:38074678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000610745
Start	38074521:38074521(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.868delC
AA Mutation	p.Arg290AlafsTer3(p.R290Afs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000610745
Start	38070934:38070934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1420G>T
AA Mutation	p.Glu474Ter(p.E474*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000610745
Start	38070810:38070810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1544C>A
AA Mutation	p.Ser515Ter(p.S515*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000610745
Start	38074635:38074636(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.753dupC
AA Mutation	p.Asn252GlnfsTer75(p.N252Qfs*75)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000610745
Start	38074520:38074521(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs587778875
CDS Mutation	c.868dupC
AA Mutation	p.Arg290ProfsTer37(p.R290Pfs*37)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CYP1B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000610745
Start	38070976:38070976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378G>T
AA Mutation	p.Val460Leu(p.V460L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000610745
Start	38070934:38070934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1420G>T
AA Mutation	p.Glu474Ter(p.E474*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript