List of variants in gene PRKRA reported as likely benign for basal ganglia disorder

Minimum submission review status:		Collection method:
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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: 22

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HGVS	dbSNP	gnomAD frequency
NM_003690.5(PRKRA):c.549T>C (p.Asn183=)	rs61746229	0.04819
NM_003690.5(PRKRA):c.66-10G>T	rs375307696	0.00024
NM_003690.5(PRKRA):c.235+11A>G	rs753131558	0.00006
NM_003690.5(PRKRA):c.261G>A (p.Ala87=)	rs778921785	0.00004
NM_003690.5(PRKRA):c.65+10C>T	rs535076601	0.00004
NM_003690.5(PRKRA):c.15G>A (p.Arg5=)
NM_003690.5(PRKRA):c.180A>G (p.Gln60=)
NM_003690.5(PRKRA):c.228C>G (p.Thr76=)
NM_003690.5(PRKRA):c.235+20C>G
NM_003690.5(PRKRA):c.285C>A (p.Ala95=)	rs546281621
NM_003690.5(PRKRA):c.309A>C (p.Ala103=)
NM_003690.5(PRKRA):c.317+14C>T
NM_003690.5(PRKRA):c.348C>T (p.Asp116=)	rs752108367
NM_003690.5(PRKRA):c.397-19C>T
NM_003690.5(PRKRA):c.435T>C (p.Tyr145=)
NM_003690.5(PRKRA):c.514+13T>C
NM_003690.5(PRKRA):c.514+15C>A
NM_003690.5(PRKRA):c.65+12G>A
NM_003690.5(PRKRA):c.65+15A>C	rs2154125656
NM_003690.5(PRKRA):c.65+18C>T
NM_003690.5(PRKRA):c.65+20G>A
NM_003690.5(PRKRA):c.84A>G (p.Thr28=)	rs1336241160

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