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TAGTAGAAATGAAAGTTCTCGGTGG[C/T]GAGACGAGAGCGGTCATGCGAGCGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600542 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC101928438 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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LOC101928438 - uncharacterized LOC101928438 | ||||||
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There are no transcripts associated with this gene. |
NR4A3 - nuclear receptor subfamily 4 group A member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006981.3 | Intron | NP_008912.2 | ||||
NM_173199.2 | Intron | NP_775291.1 | ||||
NM_173200.2 | Intron | NP_775292.1 | ||||
XM_017015162.1 | Intron | XP_016870651.1 |
Set Membership: |
HapMap |