Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
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NC_051351.1:g.21319223C>T | variant | SNP
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NC_051351.1:g.21311927A>G | variant | SNP
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NC_051351.1:g.21317311C>A | variant | SNP
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NC_051351.1:g.21319536T>A | variant | SNP
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NC_051351.1:g.21319856C>T | variant | SNP
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NC_051351.1:g.21319923G>T | variant | SNP
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NC_051351.1:g.21320246G>T | variant | SNP
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NC_051351.1:g.21320843A>G | variant | SNP
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NC_051351.1:g.21311560T>C | variant | SNP
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NC_051351.1:g.21319543A>T | variant | SNP
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