Colon Cancer: Gene >> CYP2A6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301141
Start	40847037:40847037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669C>A
AA Mutation	p.Phe223Leu(p.F223L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301141
Start	40845373:40845373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1082G>T
AA Mutation	p.Arg361Ile(p.R361I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301141
Start	40846028:40846028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901G>T
AA Mutation	p.Gly301Trp(p.G301W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301141
Start	40848649:40848649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.458C>T
AA Mutation	p.Ala153Val(p.A153V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301141
Start	40849959:40849959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143690364
CDS Mutation	c.202G>A
AA Mutation	p.Val68Met(p.V68M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301141
Start	40849854:40849854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307G>A
AA Mutation	p.Glu103Lys(p.E103K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000301141
Start	40848266:40848266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56256500
CDS Mutation	c.607C>T
AA Mutation	p.Arg203Cys(p.R203C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301141
Start	40845983:40845983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.946C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301141
Start	40845972:40845972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545581940
CDS Mutation	c.957G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301141
Start	40849864:40849864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777681590
CDS Mutation	c.297C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301141
Start	40848747:40848747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.360C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301141
Start	40848689:40848689(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.418delG
AA Mutation	p.Val140TrpfsTer35(p.V140Wfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CYP2A6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301141
Start	40848265:40848265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145393137
CDS Mutation	c.608G>A
AA Mutation	p.Arg203His(p.R203H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301141
Start	40849840:40849840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.321C>A
AA Mutation	p.Phe107Leu(p.F107L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301141
Start	40849841:40849841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.320T>A
AA Mutation	p.Phe107Tyr(p.F107Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301141
Start	40846889:40846889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817A>T
AA Mutation	p.Ile273Phe(p.I273F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301141
Start	40843899:40843899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1382G>A
AA Mutation	p.Arg461His(p.R461H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301141
Start	40850346:40850346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.81G>T
AA Mutation	p.Arg27Ser(p.R27S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript