Colon Cancer: Gene >> OSBPL9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000428468
Start	51745543:51745543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326A>T
AA Mutation	p.Asp109Val(p.D109V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000428468
Start	51772673:51772673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748634262
CDS Mutation	c.1120G>A
AA Mutation	p.Val374Ile(p.V374I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000428468
Start	51785825:51785825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1847A>G
AA Mutation	p.Lys616Arg(p.K616R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000428468
Start	51772125:51772125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776013856
CDS Mutation	c.994C>T
AA Mutation	p.Arg332Cys(p.R332C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000428468
Start	51748396:51748396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490A>C
AA Mutation	p.Asn164His(p.N164H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000428468
Start	51772140:51772140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009G>A
AA Mutation	p.Glu337Lys(p.E337K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000428468
Start	51772653:51772653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1100C>A
AA Mutation	p.Ser367Tyr(p.S367Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000428468
Start	51750174:51750174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.522T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000428468
Start	51782636:51782636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1506T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000428468
Start	51669463:51669463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OSBPL9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000428468
Start	51761882:51761882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.689G>T
AA Mutation	p.Cys230Phe(p.C230F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000428468
Start	51772689:51772689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1136T>C
AA Mutation	p.Leu379Ser(p.L379S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000428468
Start	51714060:51714060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299G>A
AA Mutation	p.Arg100Gln(p.R100Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000428468
Start	51669460:51669460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.189G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000428468
Start	51761884:51761885(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.691_692insCACACTTAAGCTATTATCGTCACAT
AA Mutation	p.Lys231ThrfsTer36(p.K231Tfs*36)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript