Colon Cancer: Gene >> OSBPL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313367
Start	24842394:24842394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286A>G
AA Mutation	p.Asn429Ser(p.N429S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313367
Start	24834601:24834601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1631C>T
AA Mutation	p.Ala544Val(p.A544V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313367
Start	24861676:24861676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.964G>T
AA Mutation	p.Gly322Cys(p.G322C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313367
Start	24863540:24863540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150182562
CDS Mutation	c.733G>A
AA Mutation	p.Val245Ile(p.V245I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313367
Start	24872060:24872060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.106G>A
AA Mutation	p.Glu36Lys(p.E36K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313367
Start	24865434:24865434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581A>C
AA Mutation	p.Gln194Pro(p.Q194P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313367
Start	24830899:24830899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1753G>C
AA Mutation	p.Val585Leu(p.V585L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000313367
Start	24863504:24863504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145677429
CDS Mutation	c.769G>A
AA Mutation	p.Ala257Thr(p.A257T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313367
Start	24852513:24852513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313367
Start	24806805:24806805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2415T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313367
Start	24800204:24800204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2643G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313367
Start	24834720:24834720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777240757
CDS Mutation	c.1512T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313367
Start	24834513:24834513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775214065
CDS Mutation	c.1719G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313367
Start	24834552:24834552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201551833
CDS Mutation	c.1680C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313367
Start	24830776:24830776(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs35793413
CDS Mutation	c.1876delT
AA Mutation	p.Ser626GlnfsTer26(p.S626Qfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000313367
Start	24830900:24830900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1752T>A
AA Mutation	p.Tyr584Ter(p.Y584*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> OSBPL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313367
Start	24852589:24852589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1073G>T
AA Mutation	p.Arg358Ile(p.R358I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313367
Start	24865445:24865445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570G>T
AA Mutation	p.Gln190His(p.Q190H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript