List of variants in gene NAA10 reported as likely pathogenic for syndromic intellectual disability

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_003491.4(NAA10):c.469G>A (p.Glu157Lys)	rs1557107264	0.00001
NM_003491.4(NAA10):c.*39A>G	rs1603289774
NM_003491.4(NAA10):c.*40A>G	rs1342269961
NM_003491.4(NAA10):c.*43A>G	rs1603289772
NM_003491.4(NAA10):c.115C>A (p.Pro39Thr)	rs1603290816
NM_003491.4(NAA10):c.116C>T (p.Pro39Leu)	rs1557107942
NM_003491.4(NAA10):c.128A>G (p.Tyr43Cys)
NM_003491.4(NAA10):c.215T>C (p.Ile72Thr)	rs1057519448
NM_003491.4(NAA10):c.235C>T (p.Arg79Cys)	rs1057524031
NM_003491.4(NAA10):c.259G>T (p.Ala87Ser)	rs1557107543
NM_003491.4(NAA10):c.295A>T (p.Ile99Leu)	rs2148535236
NM_003491.4(NAA10):c.346C>T (p.Arg116Trp)
NM_003491.4(NAA10):c.347G>A (p.Arg116Gln)	rs2065169655
NM_003491.4(NAA10):c.361C>G (p.Leu121Val)	rs1557107462
NM_003491.4(NAA10):c.377T>G (p.Leu126Arg)	rs1603290291
NM_003491.4(NAA10):c.382T>A (p.Phe128Ile)
NM_003491.4(NAA10):c.387-1G>A

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