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TATTAAATAACAAGAACCAATGGAG[A/G]GTCTAACAACTAGTAAATGACAAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605573 MIM: 609182 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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 - 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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HSD17B3 - hydroxysteroid 17-beta dehydrogenase 3 | ||||||
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There are no transcripts associated with this gene. |
SLC35D2 - solute carrier family 35 member D2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286990.1 | Intron | NP_001273919.1 | ||||
NM_007001.2 | Intron | NP_008932.2 | ||||
XM_005251673.1 | Intron | XP_005251730.1 | ||||
XM_005251674.1 | Intron | XP_005251731.1 | ||||
XM_005251675.2 | Intron | XP_005251732.1 | ||||
XM_005251676.1 | Intron | XP_005251733.1 | ||||
XM_005251678.4 | Intron | XP_005251735.1 | ||||
XM_006716939.2 | Intron | XP_006717002.1 | ||||
XM_011518164.1 | Intron | XP_011516466.1 |
Set Membership: |
HapMap |