Colon Cancer: Gene >> CYP46A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261835
Start	99715859:99715859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762967586
CDS Mutation	c.743G>A
AA Mutation	p.Arg248His(p.R248H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261835
Start	99726575:99726575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1351A>G
AA Mutation	p.Met451Val(p.M451V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261835
Start	99718094:99718094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.948G>A
AA Mutation	p.Met316Ile(p.M316I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261835
Start	99715853:99715853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.737G>T
AA Mutation	p.Ser246Ile(p.S246I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261835
Start	99715887:99715887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.771G>T
AA Mutation	p.Trp257Cys(p.W257C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261835
Start	99726225:99726225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1301A>C
AA Mutation	p.His434Pro(p.H434P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261835
Start	99700084:99700084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.426C>A
AA Mutation	p.Asp142Glu(p.D142E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261835
Start	99726624:99726624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1400G>A
AA Mutation	p.Arg467His(p.R467H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261835
Start	99726196:99726196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1272G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261835
Start	99700069:99700069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.411G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261835
Start	99706656:99706656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.453T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261835
Start	99716195:99716195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.903T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261835
Start	99726628:99726628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749061350
CDS Mutation	c.1404C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CYP46A1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261835
Start	99691843:99691843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000261835
Start	99725426:99725426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1212C>A
AA Mutation	p.Tyr404Ter(p.Y404*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript