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CTGCGTGTCTGACGGAGAAGGGGGC[C/T]GAGCAGCTGAGGGGCCAGACGTCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606623 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HSD17B6 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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HSD17B6 - hydroxysteroid 17-beta dehydrogenase 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003725.3 | 538 | Silent Mutation | GCC,GCT | A,A 66 | NP_003716.2 | |
XM_005269207.1 | 538 | Silent Mutation | GCC,GCT | A,A 66 | XP_005269264.1 | |
XM_005269208.1 | 538 | Silent Mutation | GCC,GCT | A,A 66 | XP_005269265.1 | |
XM_005269209.1 | 538 | Silent Mutation | GCC,GCT | A,A 66 | XP_005269266.1 | |
XM_006719672.1 | 538 | Silent Mutation | GCC,GCT | A,A 66 | XP_006719735.1 | |
XM_011538925.1 | 538 | Silent Mutation | GCC,GCT | A,A 66 | XP_011537227.1 | |
XM_011538926.1 | 538 | Silent Mutation | GCC,GCT | A,A 66 | XP_011537228.1 | |
XM_011538927.1 | 538 | Silent Mutation | GCC,GCT | A,A 66 | XP_011537229.1 |