List of variants in gene combination DNM1, LOC113839516 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)
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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_004408.4(DNM1):c.312G>A (p.Glu104=)	rs2229917	0.11354
NM_004408.4(DNM1):c.357T>C (p.Pro119=)	rs77325628	0.00468
NM_004408.4(DNM1):c.386-14G>A	rs141695422	0.00189
NM_004408.4(DNM1):c.450C>G (p.Pro150=)	rs143834670	0.00093
NM_004408.4(DNM1):c.332C>G (p.Thr111Ser)	rs192913494	0.00066
NM_004408.4(DNM1):c.261G>A (p.Lys87=)	rs377178808	0.00002
NM_004408.4(DNM1):c.474C>T (p.Asp158=)	rs568247101	0.00001
NM_004408.4(DNM1):c.543G>A (p.Leu181=)	rs759118746	0.00001

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