List of variants in gene ATP5F1D, LOC130062904 studied for Inborn genetic diseases

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001687.5(ATP5F1D):c.452C>T (p.Ala151Val)	rs200485963	0.00014
NM_001687.5(ATP5F1D):c.496G>T (p.Ala166Ser)	rs373551178	0.00005
NM_001687.5(ATP5F1D):c.481G>A (p.Glu161Lys)	rs370466468	0.00004
NM_001687.5(ATP5F1D):c.406A>G (p.Lys136Glu)	rs750127098	0.00001
NM_001687.5(ATP5F1D):c.434C>A (p.Ala145Asp)	rs989928611
NM_001687.5(ATP5F1D):c.448C>T (p.Arg150Trp)	rs201886813
NM_001687.5(ATP5F1D):c.467G>A (p.Arg156Gln)

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