ClinVar Miner

List of variants in gene NAA10 reported as uncertain significance for X-linked disease

Included ClinVar conditions (275):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_003491.4(NAA10):c.534C>A (p.Asn178Lys) rs1360898468 0.00001
NM_003491.4(NAA10):c.112T>G (p.Trp38Gly) rs2148536647
NM_003491.4(NAA10):c.303C>A (p.Asn101Lys) rs781871487
NM_003491.4(NAA10):c.303C>G (p.Asn101Lys) rs781871487
NM_003491.4(NAA10):c.30C>G (p.Asp10Glu) rs2148536720
NM_003491.4(NAA10):c.418G>T (p.Asp140Tyr) rs2148534337
NM_003491.4(NAA10):c.430G>A (p.Ala144Thr) rs2065162376
NM_003491.4(NAA10):c.445C>T (p.Arg149Trp) rs2065162324

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