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TGTAATTTCAAGCAGTAAAATCATA[A/T]TTTAGGAAACAAAGAATGCACACTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613214 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
WDR72 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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WDR72 - WD repeat domain 72 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001277176.1 | 5026 | UTR 3 | NP_001264105.1 | |||
NM_182758.3 | 5026 | UTR 3 | NP_877435.3 | |||
XM_011521433.2 | 5026 | UTR 3 | XP_011519735.1 | |||
XM_011521435.2 | 5026 | UTR 3 | XP_011519737.1 | |||
XM_011521436.2 | 5026 | Intron | XP_011519738.1 | |||
XM_011521437.2 | 5026 | Intron | XP_011519739.1 | |||
XM_017022061.1 | 5026 | UTR 3 | XP_016877550.1 |