ClinVar Miner

Variants in gene DNAAF2 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 7
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HGVS dbSNP
NM_018139.2(DNAAF2):c.129C>T (p.Leu43=) rs567371975
NM_018139.2(DNAAF2):c.1367C>T (p.Pro456Leu) rs137991407
NM_018139.2(DNAAF2):c.1406G>A (p.Cys469Tyr) rs150737854
NM_018139.2(DNAAF2):c.1584T>A (p.Asn528Lys) rs144077436
NM_018139.2(DNAAF2):c.561C>T (p.Thr187=) rs529083217
NM_018139.2(DNAAF2):c.707C>T (p.Pro236Leu) rs74050429
NM_018139.2(DNAAF2):c.78C>T (p.Ala26=) rs7156297

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