Colon Cancer: Gene >> OSBPL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313733
Start	62289294:62289294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1213C>T
AA Mutation	p.Arg405Cys(p.R405C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313733
Start	62272189:62272189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.323C>T
AA Mutation	p.Thr108Met(p.T108M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313733
Start	62279327:62279327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662T>C
AA Mutation	p.Leu221Pro(p.L221P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313733
Start	62281824:62281824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.817T>G
AA Mutation	p.Cys273Gly(p.C273G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313733
Start	62281097:62281097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748360123
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313733
Start	62279202:62279202(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.543delC
AA Mutation	p.Ile182SerfsTer68(p.I182Sfs*68)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313733
Start	62293820:62293820(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1380delC
AA Mutation	p.Asp461ThrfsTer44(p.D461Tfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000313733
Start	62284079:62284079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.906G>A
AA Mutation	p.Trp302Ter(p.W302*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313733
Start	62279201:62279202(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs780916980
CDS Mutation	c.543dupC
AA Mutation	p.Ile182HisfsTer12(p.I182Hfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> OSBPL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313733
Start	62273331:62273331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767753104
CDS Mutation	c.416C>T
AA Mutation	p.Ser139Leu(p.S139L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313733
Start	62289256:62289256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753787827
CDS Mutation	c.1175G>A
AA Mutation	p.Gly392Asp(p.G392D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript