ClinVar Miner

List of variants in gene PURA reported as likely pathogenic for PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation

Included ClinVar conditions (2):
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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_005859.5(PURA):c.-12_25del (p.Met1fs) rs1763033823
NM_005859.5(PURA):c.15del (p.Asp5fs) rs2126748515
NM_005859.5(PURA):c.190A>T (p.Lys64Ter)
NM_005859.5(PURA):c.1A>G (p.Met1Val) rs793888530
NM_005859.5(PURA):c.215G>C (p.Arg72Pro)
NM_005859.5(PURA):c.227A>C (p.Asp76Ala)
NM_005859.5(PURA):c.227A>T (p.Asp76Val)
NM_005859.5(PURA):c.259A>G (p.Lys87Glu)
NM_005859.5(PURA):c.265G>C (p.Ala89Pro) rs587782999
NM_005859.5(PURA):c.273_328del (p.Gly92fs)
NM_005859.5(PURA):c.298_315del (p.Leu100_Ser105del) rs1763043820
NM_005859.5(PURA):c.299T>C (p.Leu100Pro) rs587782995
NM_005859.5(PURA):c.305T>C (p.Leu102Pro) rs793888531
NM_005859.5(PURA):c.449_456del (p.Arg150fs) rs1581036405
NM_005859.5(PURA):c.45_60dup (p.Leu21fs) rs1581036015
NM_005859.5(PURA):c.469A>G (p.Met157Val) rs2126749113
NM_005859.5(PURA):c.493G>A (p.Gly165Ser) rs1561793272
NM_005859.5(PURA):c.496C>T (p.Arg166Cys) rs1554129096
NM_005859.5(PURA):c.4_7dup (p.Asp3fs)
NM_005859.5(PURA):c.503T>C (p.Leu168Pro) rs1581036449
NM_005859.5(PURA):c.50C>A (p.Ser17Ter) rs1346561117
NM_005859.5(PURA):c.50del (p.Ser17fs) rs1554129008
NM_005859.5(PURA):c.511C>G (p.Arg171Gly) rs1554129100
NM_005859.5(PURA):c.540_544dup (p.Ser182fs)
NM_005859.5(PURA):c.563T>C (p.Ile188Thr) rs793888527
NM_005859.5(PURA):c.563_578del (p.Ile188fs) rs2126749241
NM_005859.5(PURA):c.565G>C (p.Ala189Pro) rs1581036496
NM_005859.5(PURA):c.577C>T (p.Gln193Ter)
NM_005859.5(PURA):c.586_588del (p.Ile196del)
NM_005859.5(PURA):c.596G>C (p.Arg199Pro) rs587783001
NM_005859.5(PURA):c.605T>C (p.Leu202Pro) rs1561793336
NM_005859.5(PURA):c.614T>C (p.Leu205Pro) rs1581036537
NM_005859.5(PURA):c.657del (p.Glu220fs)
NM_005859.5(PURA):c.66del (p.His23fs) rs1581036051
NM_005859.5(PURA):c.710C>T (p.Ser237Phe) rs886039899
NM_005859.5(PURA):c.779C>G (p.Pro260Arg) rs1064795567
NM_005859.5(PURA):c.824C>A (p.Ser275Ter) rs2126749442

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