ClinVar Miner

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

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 7
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HGVS dbSNP
NM_018139.2(DNAAF2):c.1405T>A (p.Cys469Ser) rs202079418
NM_018139.2(DNAAF2):c.1406G>A (p.Cys469Tyr) rs150737854
NM_018139.2(DNAAF2):c.1687G>T (p.Ala563Ser) rs138511448
NM_018139.2(DNAAF2):c.20C>T (p.Ser7Phe) rs577796590
NM_018139.2(DNAAF2):c.423C>T (p.Val141=) rs373251065
NM_018139.2(DNAAF2):c.561C>T (p.Thr187=) rs529083217
NM_018139.2(DNAAF2):c.58G>C (p.Val20Leu) rs572322476

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