List of variants in gene PRICKLE1 reported as benign for adolescent-onset epilepsy syndrome

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_153026.3(PRICKLE1):c.1902T>C (p.Ser634=)	rs3747562	0.45408
NM_153026.3(PRICKLE1):c.1899T>C (p.Phe633=)	rs3747563	0.32044
NM_153026.3(PRICKLE1):c.585C>T (p.Asp195=)	rs74081707	0.03104
NM_153026.3(PRICKLE1):c.744G>A (p.Ala248=)	rs34778200	0.01220
NM_153026.3(PRICKLE1):c.2236C>T (p.Pro746Ser)	rs3827522	0.00701
NM_153026.3(PRICKLE1):c.374T>C (p.Val125Ala)	rs34837068	0.00631
NM_153026.3(PRICKLE1):c.2304C>G (p.Ser768=)	rs35854729	0.00598
NM_153026.3(PRICKLE1):c.370G>A (p.Ala124Thr)	rs79087668	0.00498
NM_153026.3(PRICKLE1):c.108C>T (p.Val36=)	rs147268650	0.00376
NM_153026.3(PRICKLE1):c.114G>A (p.Pro38=)	rs141743294	0.00302
NM_153026.3(PRICKLE1):c.177C>T (p.Tyr59=)	rs144843013	0.00149
NM_153026.3(PRICKLE1):c.1461C>T (p.Ser487=)	rs116197349	0.00121
NM_153026.3(PRICKLE1):c.1869G>A (p.Lys623=)	rs150809651	0.00003
NM_153026.3(PRICKLE1):c.373G>A (p.Val125Met)
NM_153026.3(PRICKLE1):c.588+10dup	rs766626651

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