Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
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NC_051336.1:g.207326299A>G | variant | SNP
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NC_051336.1:g.207315734G>A | variant | SNP
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NC_051336.1:g.207316375C>T | variant | SNP
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NC_051336.1:g.207318139C>T | variant | SNP
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NC_051336.1:g.207320297A>G | variant | SNP
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NC_051336.1:g.207320969A>G | variant | SNP
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NC_051336.1:g.207321960G>C | variant | SNP
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NC_051336.1:g.207306284A>G | variant | SNP
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NC_051336.1:g.207313743A>G | variant | SNP
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NC_051336.1:g.207320481C>G | variant | SNP
|