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TGCAAAATTTAAGAAGACATTCACT[A/T]CCAGGTTCCTGGTCCTGGAAGCCTC
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 |
---|---|---|
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 |
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 |