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- SNP ID:
- rs12591557
- Gene
-
HYKK - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.15: 78519390 - 78519390 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
AAAATGTTCATTTGTTCACAATAAT[A/G]TAAGTTGGATTTAAATAGCCCTTTC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614681
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Literature Links: |
HYKK PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | ||||||
|---|---|---|---|---|---|---|---|---|
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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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| HYKK - hydroxylysine kinase | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001013619.3 | Intron | NP_001013641.2 | ||||
| NM_001083612.1 | Intron | NP_001077081.1 | ||||
| XM_011521231.2 | Intron | XP_011519533.1 | ||||
| XM_017021922.1 | Intron | XP_016877411.1 | ||||
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