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ATCTAGTTGGAAATAAAGGTCAGCT[G/T]TTGTTTAGGCACCATTGTGTAAGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603826 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NR1H4 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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NR1H4 - nuclear receptor subfamily 1 group H member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001206977.1 | Intron | NP_001193906.1 | ||||
NM_001206978.1 | Intron | NP_001193907.1 | ||||
NM_001206979.1 | Intron | NP_001193908.1 | ||||
NM_001206992.1 | Intron | NP_001193921.1 | ||||
NM_001206993.1 | Intron | NP_001193922.1 | ||||
NM_005123.3 | Intron | NP_005114.1 | ||||
XM_006719719.2 | Intron | XP_006719782.1 | ||||
XM_011539040.2 | Intron | XP_011537342.1 | ||||
XM_011539041.2 | Intron | XP_011537343.1 | ||||
XM_011539042.1 | Intron | XP_011537344.1 |