Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616163 MIM: 610418 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
DHRS12 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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DHRS12 - dehydrogenase/reductase 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031719.2 | 655 | Intron | NP_001026889.1 | |||
NM_001270424.1 | 655 | Missense Mutation | AGG,GGG | R,G 249 | NP_001257353.1 | |
NM_024705.2 | 655 | Missense Mutation | AGG,GGG | R,G 200 | NP_078981.1 | |
XM_005266527.3 | 655 | Missense Mutation | AGG,GGG | R,G 200 | XP_005266584.1 | |
XM_005266528.4 | 655 | Intron | XP_005266585.1 | |||
XM_011535235.2 | 655 | Intron | XP_011533537.1 | |||
XM_011535236.2 | 655 | Intron | XP_011533538.1 | |||
XM_011535237.1 | 655 | Intron | XP_011533539.1 | |||
XM_011535238.1 | 655 | Intron | XP_011533540.1 | |||
XM_017020749.1 | 655 | Intron | XP_016876238.1 | |||
XM_017020750.1 | 655 | Intron | XP_016876239.1 | |||
XM_017020751.1 | 655 | Intron | XP_016876240.1 | |||
XM_017020752.1 | 655 | Intron | XP_016876241.1 | |||
XM_017020753.1 | 655 | Intron | XP_016876242.1 | |||
XM_017020754.1 | 655 | Missense Mutation | AGG,GGG | R,G 104 | XP_016876243.1 |
WDFY2 - WD repeat and FYVE domain containing 2 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |