Colon Cancer: Gene >> OSBPL1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319481
Start	24332996:24332996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571T>G
AA Mutation	p.Cys191Gly(p.C191G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319481
Start	24368331:24368331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.163G>T
AA Mutation	p.Ala55Ser(p.A55S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000319481
Start	24312105:24312105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.971A>G
AA Mutation	p.Asp324Gly(p.D324G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319481
Start	24239302:24239302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1362T>A
AA Mutation	p.His454Gln(p.H454Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319481
Start	24165105:24165105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754928699
CDS Mutation	c.2710C>T
AA Mutation	p.Arg904Cys(p.R904C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000319481
Start	24239231:24239231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1433A>C
AA Mutation	p.Asp478Ala(p.D478A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000319481
Start	24368346:24368346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.148A>G
AA Mutation	p.Thr50Ala(p.T50A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319481
Start	24314309:24314309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.909C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319481
Start	24179788:24179788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1860G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319481
Start	24166590:24166590(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2648delA
AA Mutation	p.Asn883MetfsTer4(p.N883Mfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319481
Start	24165133:24165133(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2682delA
AA Mutation	p.Lys894AsnfsTer71(p.K894Nfs*71)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000319481
Start	24179794:24179794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1854G>A
AA Mutation	p.Trp618Ter(p.W618*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319481
Start	24170366:24170367(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2378dupA
AA Mutation	p.Asn793LysfsTer2(p.N793Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> OSBPL1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319481
Start	24166698:24166698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2540A>G
AA Mutation	p.Tyr847Cys(p.Y847C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319481
Start	24377493:24377493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.41G>T
AA Mutation	p.Arg14Ile(p.R14I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript