List of variants in gene UNC13D reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_199242.3(UNC13D):c.2341G>A (p.Val781Ile)	rs149871493	0.00161
NM_199242.3(UNC13D):c.610A>G (p.Met204Val)	rs144722609	0.00081
NM_199242.3(UNC13D):c.3160A>G (p.Ile1054Val)	rs150952348	0.00051
NM_199242.3(UNC13D):c.887C>T (p.Pro296Leu)	rs541737648	0.00019
NM_199242.3(UNC13D):c.467G>A (p.Arg156Gln)	rs370610759	0.00009
NM_199242.3(UNC13D):c.794C>G (p.Pro265Arg)	rs200265541	0.00007
NM_199242.3(UNC13D):c.1477G>A (p.Gly493Ser)	rs759754878	0.00003
NM_199242.3(UNC13D):c.3079G>A (p.Gly1027Arg)	rs776703437	0.00001
NM_199242.3(UNC13D):c.3149A>G (p.Asn1050Ser)	rs754299432	0.00001
NM_199242.3(UNC13D):c.1807G>A (p.Glu603Lys)	rs755348845
NM_199242.3(UNC13D):c.2346_2349del (p.Arg782fs)	rs764196809
NM_199242.3(UNC13D):c.70C>G (p.Arg24Gly)	rs749234163

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