List of variants in gene KIAA1549 reported as benign for inborn disorder of amino acid metabolism

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001164665.2(KIAA1549):c.3708G>T (p.Pro1236=)	rs7802841	0.71421
NM_001164665.2(KIAA1549):c.2973C>T (p.Tyr991=)	rs6969074	0.54454
NM_001164665.2(KIAA1549):c.1849A>G (p.Arg617Gly)	rs2774962	0.52408
NM_001164665.2(KIAA1549):c.2546C>T (p.Ser849Leu)	rs2251220	0.43675
NM_001164665.2(KIAA1549):c.1955C>T (p.Pro652Leu)	rs2774960	0.41799
NM_001164665.2(KIAA1549):c.2301T>C (p.Thr767=)	rs61746879	0.08707
NM_001164665.2(KIAA1549):c.2800G>A (p.Asp934Asn)	rs2150283	0.05297
NM_001164665.2(KIAA1549):c.2666G>T (p.Gly889Val)	rs2354336	0.05287
NM_001164665.2(KIAA1549):c.1940C>G (p.Ser647Cys)	rs61734132	0.05285
NM_001164665.2(KIAA1549):c.1090A>G (p.Thr364Ala)	rs59985563
NM_001164665.2(KIAA1549):c.2316C>T (p.Pro772=)	rs61746877

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