Colon Cancer: Gene >> SCARB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000415380
Start	124807871:124807871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.899G>T
AA Mutation	p.Arg300Leu(p.R300L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000415380
Start	124817554:124817554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280T>C
AA Mutation	p.Tyr94His(p.Y94H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000415380
Start	124811892:124811892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.704A>G
AA Mutation	p.Asp235Gly(p.D235G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000415380
Start	124795229:124795229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369260422
CDS Mutation	c.1168C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000415380
Start	124807801:124807801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000415380
Start	124817591:124817591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775911956
CDS Mutation	c.243C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000415380
Start	124817582:124817582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776876716
CDS Mutation	c.252G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SCARB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000415380
Start	124817695:124817695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371712274
CDS Mutation	c.139G>A
AA Mutation	p.Asp47Asn(p.D47N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript