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CGGTCCAGGCGTTTGAAGTCAAGAC[A/G]TCCCCGACAGTGGGCAGCTGAGGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616157 MIM: 131560 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DHRS13 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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DHRS13 - dehydrogenase/reductase 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_144683.3 | 656 | Missense Mutation | CGT,TGT | R,C 177 | NP_653284.2 |
FLOT2 - flotillin 2 | ||||||
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There are no transcripts associated with this gene. |
PHF12 - PHD finger protein 12 | ||||||
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There are no transcripts associated with this gene. |