Colon Cancer: Gene >> CYP11A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268053
Start	74348000:74348000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325C>A
AA Mutation	p.Leu109Ile(p.L109I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268053
Start	74343121:74343121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.846G>T
AA Mutation	p.Gln282His(p.Q282H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268053
Start	74343001:74343001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.966G>T
AA Mutation	p.Glu322Asp(p.E322D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268053
Start	74342993:74342993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.974C>T
AA Mutation	p.Ala325Val(p.A325V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268053
Start	74343078:74343078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777640411
CDS Mutation	c.889G>A
AA Mutation	p.Asp297Asn(p.D297N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268053
Start	74343835:74343835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.783G>T
AA Mutation	p.Lys261Asn(p.K261N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268053
Start	74343982:74343982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs6160
CDS Mutation	c.636C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268053
Start	74345231:74345231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268053
Start	74347986:74347986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761284043
CDS Mutation	c.339C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268053
Start	74338020:74338020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1518C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268053
Start	74367517:74367517(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.69delC
AA Mutation	p.Arg24GlyfsTer37(p.R24Gfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CYP11A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268053
Start	74345107:74345107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.562A>G
AA Mutation	p.Lys188Glu(p.K188E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript