Does anyone know how to check sequenced nucleotide variants against known disease variants?
In HGMD the variant coordinates are by codon position with the cDNA. Is there a way to map this information to genomic coordinates? Is there a more useful database out there?
In HGMD the variant coordinates are by codon position with the cDNA. Is there a way to map this information to genomic coordinates? Is there a more useful database out there?
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