List of variants in gene DNM1L reported as uncertain significance for not specified

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_012062.5(DNM1L):c.305C>T (p.Thr102Met)	rs201929226	0.00026
NM_012062.5(DNM1L):c.1255C>T (p.Arg419Trp)	rs776779003
NM_012062.5(DNM1L):c.1582G>A (p.Val528Ile)	rs778877877
NM_012062.5(DNM1L):c.471T>G (p.Asp157Glu)
NM_012062.5(DNM1L):c.889A>T (p.Ile297Phe)	rs2541045651

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