Product Details

SNP ID

rs143626823

Assay Type

Functionally tested

NCBI dbSNP Submissions

16

Location

Chr.1:51617209 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCTGGACTACAATGCAGGACTGCT[C/T]TCCTACTACACGGTGAGTCCTTGGA

Phenotype

MIM: 606737

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

OSBPL9 PubMed Links

Gene Details

Gene

OSBPL9

Gene Name

oxysterol binding protein like 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024586.5	118	Silent Mutation	CTC,CTT	L33L	NP_078862.4
NM_148904.3	118	Intron			NP_683702.1
NM_148905.3	118	Intron			NP_683703.1
NM_148906.2	118	Silent Mutation	CTC,CTT	L33L	NP_683704.2
NM_148907.2	118	Intron			NP_683705.1
NM_148908.3	118	Silent Mutation	CTC,CTT	L33L	NP_683706.3
NM_148909.3	118	Silent Mutation	CTC,CTT	L33L	NP_683707.3
XM_006710318.2	118	Silent Mutation	CTC,CTT	L33L	XP_006710381.1
XM_006710320.3	118	Intron			XP_006710383.1
XM_006710321.2	118	Intron			XP_006710384.1
XM_006710322.3	118	Intron			XP_006710385.1
XM_006710323.2	118	Intron			XP_006710386.1
XM_006710324.3	118	UTR 5			XP_006710387.1
XM_006710325.3	118	UTR 5			XP_006710388.1
XM_006710326.2	118	Intron			XP_006710389.1
XM_011540599.2	118	Silent Mutation	CTC,CTT	L33L	XP_011538901.1
XM_011540600.2	118	Silent Mutation	CTC,CTT	L33L	XP_011538902.1
XM_011540601.2	118	Silent Mutation	CTC,CTT	L33L	XP_011538903.1
XM_011540602.2	118	Intron			XP_011538904.1
XM_011540603.2	118	UTR 5			XP_011538905.1
XM_011540604.2	118	Intron			XP_011538906.1
XM_017000218.1	118	Silent Mutation	CTC,CTT	L33L	XP_016855707.1
XM_017000219.1	118	UTR 5			XP_016855708.1
XM_017000220.1	118	Intron			XP_016855709.1
XM_017000221.1	118	Intron			XP_016855710.1
XM_017000222.1	118	UTR 5			XP_016855711.1
XM_017000223.1	118	UTR 5			XP_016855712.1
XM_017000224.1	118	Intron			XP_016855713.1
XM_017000225.1	118	Intron			XP_016855714.1

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