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- SNP ID:
- rs12478071
- Gene
-
NCOA1 - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.2: 24500875 - 24500875 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
AACAACAAAAAATTTAATGCTGTAG[A/G]GAAAGGATATTGAAAATGGATATTT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602691
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Literature Links: |
NCOA1 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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| NCOA1 - nuclear receptor coactivator 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_003743.4 | Intron | NP_003734.3 | ||||
| NM_147223.2 | Intron | NP_671756.1 | ||||
| NM_147233.2 | Intron | NP_671766.1 | ||||
| XM_005264625.1 | Intron | XP_005264682.1 | ||||
| XM_005264626.1 | Intron | XP_005264683.1 | ||||
| XM_005264628.1 | Intron | XP_005264685.1 | ||||
| XM_017005168.1 | Intron | XP_016860657.1 | ||||
| XM_017005169.1 | Intron | XP_016860658.1 | ||||
Back To TopMore Information
Set Membership: |
HapMap
|
Panther Classification:
Gene Ontology Categories:
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