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disease: not specified

id16789
namenot specified
descriptionThe term 'not specified' was created for use in ClinVar so that submitters can convey the concept that a variant is benign, likely benign, or of uncertain significance for an unspecified set of disorders. This usage was introduced in 2014 to replace AllHighlyPenetrant.
variant-disease NM_007294.3(BRCA1):c.1974G>C (p.Met658Ile) AND not specified
NM_007299.4(BRCA1):c.788-1830G>T AND not specified
NM_007294.3(BRCA1):c.3415_3417AGT[1] (p.Ser1140del) AND not specified
NM_007294.3(BRCA1):c.3691T>C (p.Phe1231Leu) AND not specified
NM_007294.3(BRCA1):c.3739G>A (p.Val1247Ile) AND not specified
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