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TAGGGAGGCTTCAGTTCTGGTTCTA[C/G]GTGGACCTCTCAGACACCCTGGGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 180240 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC105371934 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 | 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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LOC105371934 - uncharacterized LOC105371934 | ||||||
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There are no transcripts associated with this gene. |
RARA - retinoic acid receptor alpha | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000964.3 | Intron | NP_000955.1 | ||||
NM_001024809.3 | Intron | NP_001019980.1 | ||||
NM_001145301.2 | Intron | NP_001138773.1 | ||||
NM_001145302.2 | Intron | NP_001138774.1 | ||||
XM_005257552.4 | Intron | XP_005257609.1 | ||||
XM_005257553.1 | Intron | XP_005257610.1 | ||||
XM_005257554.1 | Intron | XP_005257611.1 | ||||
XM_011525095.1 | Intron | XP_011523397.1 | ||||
XM_011525096.1 | Intron | XP_011523398.1 | ||||
XM_017024920.1 | Intron | XP_016880409.1 |
Set Membership: |
HapMap |