List of variants in gene HACD1 reported as uncertain significance for Inborn genetic diseases

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_014241.4(HACD1):c.412G>A (p.Val138Met)	rs141646017	0.00013
NM_014241.4(HACD1):c.287G>A (p.Arg96His)	rs150586011	0.00009
NM_014241.4(HACD1):c.341C>T (p.Thr114Ile)	rs1014885693	0.00005
NM_014241.4(HACD1):c.459G>T (p.Trp153Cys)	rs782699505	0.00002
NM_014241.4(HACD1):c.322T>C (p.Tyr108His)	rs1834107555	0.00001
NM_014241.4(HACD1):c.473G>T (p.Ser158Ile)	rs781827306	0.00001
NM_014241.4(HACD1):c.545G>A (p.Arg182His)	rs1554816285	0.00001
NM_014241.4(HACD1):c.659C>T (p.Thr220Ile)	rs2493849255	0.00001
NM_014241.4(HACD1):c.427G>T (p.Val143Phe)
NM_014241.4(HACD1):c.832C>T (p.Leu278Phe)
NM_014241.4(HACD1):c.844G>A (p.Val282Met)
NM_014241.4(HACD1):c.860A>G (p.Asp287Gly)

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