ClinVar Miner

Variants in gene DEAF1 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 9
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HGVS dbSNP gnomAD frequency
NM_021008.4(DEAF1):c.1634C>G (p.Ala545Gly) rs34114147 0.00680
NM_021008.4(DEAF1):c.825C>T (p.His275=) rs144498322 0.00310
NM_021008.4(DEAF1):c.727A>G (p.Met243Val) rs71469813 0.00284
NM_021008.4(DEAF1):c.162G>C (p.Ser54=) rs141389829 0.00133
NM_021008.4(DEAF1):c.231C>T (p.Asp77=) rs371538775 0.00130
NM_021008.4(DEAF1):c.517+8G>A rs369913079 0.00048
NM_021008.4(DEAF1):c.855C>T (p.Cys285=) rs373861624 0.00036
NM_021008.4(DEAF1):c.1182C>T (p.Tyr394=) rs202179285 0.00014
NM_021008.4(DEAF1):c.1114G>A (p.Ala372Thr) rs371467345 0.00001

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