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GGAGTGAGGGCAGGAGGATACAGGT[C/T]AGAGACTCCACAAACCTTTACTGGT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
30 submissions
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Phenotype: |
MIM: 607786 MIM: 610569 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
PCSK9 PubMed Links | |||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese)
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EUR
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AMR
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PCSK9 - proprotein convertase subtilisin/kexin type 9 | ||||||
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There are no transcripts associated with this gene. |
USP24 - ubiquitin specific peptidase 24 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015306.2 | Intron | NP_056121.2 | ||||
XM_005270690.3 | Intron | XP_005270747.1 | ||||
XM_017000831.1 | Intron | XP_016856320.1 | ||||
XM_017000832.1 | Intron | XP_016856321.1 | ||||
XM_017000833.1 | Intron | XP_016856322.1 | ||||
XM_017000834.1 | Intron | XP_016856323.1 | ||||
XM_017000835.1 | Intron | XP_016856324.1 | ||||
XM_017000836.1 | Intron | XP_016856325.1 | ||||
XM_017000837.1 | Intron | XP_016856326.1 |
Set Membership: |
HapMap |