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GTGGGACATGGGGGTTGGAGGGTGG[G/T]GATGCTGCAGGGATGGTGATGGAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 606729 | ||||||||||||||||||||
Literature Links: |
OSBP2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
OSBP2 - oxysterol binding protein 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282738.1 | Intron | NP_001269667.1 | ||||
NM_001282739.1 | Intron | NP_001269668.1 | ||||
NM_001282740.1 | Intron | NP_001269669.1 | ||||
NM_001282741.1 | Intron | NP_001269670.1 | ||||
NM_001282742.1 | Intron | NP_001269671.1 | ||||
NM_030758.3 | Intron | NP_110385.1 | ||||
XM_005261465.4 | Intron | XP_005261522.1 | ||||
XM_006724203.2 | Intron | XP_006724266.2 | ||||
XM_006724207.2 | Intron | XP_006724270.1 | ||||
XM_006724208.3 | Intron | XP_006724271.1 | ||||
XM_011530057.1 | Intron | XP_011528359.1 | ||||
XM_011530058.1 | Intron | XP_011528360.1 | ||||
XM_011530059.2 | Intron | XP_011528361.1 | ||||
XM_011530060.1 | Intron | XP_011528362.1 | ||||
XM_011530061.1 | Intron | XP_011528363.1 | ||||
XM_011530062.1 | Intron | XP_011528364.1 | ||||
XM_017028708.1 | Intron | XP_016884197.1 | ||||
XM_017028709.1 | Intron | XP_016884198.1 | ||||
XM_017028710.1 | Intron | XP_016884199.1 | ||||
XM_017028711.1 | Intron | XP_016884200.1 | ||||
XM_017028712.1 | Intron | XP_016884201.1 | ||||
XM_017028713.1 | Intron | XP_016884202.1 |