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TCCCGCCTCGCAACGCCTCCTCTGC[A/G]CCAGGGCCAGGGCCTCTCCCCCTAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611237 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
BTBD9 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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BTBD9 - BTB domain containing 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099272.1 | 7816 | UTR 3 | NP_001092742.1 | |||
NM_001172418.1 | 7816 | UTR 3 | NP_001165889.1 | |||
NM_052893.1 | 7816 | UTR 3 | NP_443125.1 | |||
NM_152733.2 | 7816 | UTR 3 | NP_689946.2 | |||
XM_011514279.2 | 7816 | UTR 3 | XP_011512581.1 | |||
XM_011514280.2 | 7816 | Intron | XP_011512582.1 | |||
XM_011514281.2 | 7816 | Intron | XP_011512583.1 | |||
XM_011514282.2 | 7816 | Intron | XP_011512584.1 | |||
XM_017010227.1 | 7816 | Intron | XP_016865716.1 |