Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605573 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
HSD17B3 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
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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HSD17B3 - hydroxysteroid 17-beta dehydrogenase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000197.1 | 3297 | Missense Mutation | CGT,TGT | R,C 289 | NP_000188.1 | |
XM_011518618.2 | 3297 | Missense Mutation | CGT,TGT | R,C 289 | XP_011516920.1 | |
XM_011518619.2 | 3297 | Missense Mutation | CGT,TGT | R,C 289 | XP_011516921.1 | |
XM_017014671.1 | 3297 | Missense Mutation | CGT,TGT | R,C 289 | XP_016870160.1 | |
XM_017014672.1 | 3297 | Missense Mutation | CGT,TGT | R,C 289 | XP_016870161.1 | |
XM_017014673.1 | 3297 | Missense Mutation | CGT,TGT | R,C 277 | XP_016870162.1 | |
XM_017014674.1 | 3297 | Missense Mutation | CGT,TGT | R,C 253 | XP_016870163.1 | |
XM_017014675.1 | 3297 | Missense Mutation | CGT,TGT | R,C 235 | XP_016870164.1 | |
XM_017014676.1 | 3297 | Intron | XP_016870165.1 | |||
XM_017014677.1 | 3297 | Missense Mutation | CGT,TGT | R,C 169 | XP_016870166.1 |