List of variants in gene RP1 reported as benign for inborn disorder of amino acid metabolism

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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_006269.2(RP1):c.2953A>T (p.Asn985Tyr)	rs2293869	0.33006
NM_006269.2(RP1):c.2615G>A (p.Arg872His)	rs444772	0.24558
NM_006269.2(RP1):c.4784G>A (p.Arg1595Gln)	rs35084330	0.03211
NM_006269.2(RP1):c.3699C>T (p.Ser1233=)	rs114557304	0.03129
NM_006269.2(RP1):c.1118C>T (p.Thr373Ile)	rs77775126	0.00985
NM_006269.2(RP1):c.*72G>A	rs73679499	0.00870
NM_006269.2(RP1):c.2255C>T (p.Thr752Met)	rs28399531	0.00832
NM_006269.2(RP1):c.2991T>C (p.Asn997=)	rs112667487	0.00829
NM_006269.2(RP1):c.2833G>T (p.Val945Leu)	rs16920621	0.00690
NM_006269.2(RP1):c.616-6T>C	rs186571865	0.00458
NM_006269.2(RP1):c.*71C>T	rs185876566	0.00028
NM_006269.2(RP1):c.3999C>T (p.Tyr1333=)	rs146602041	0.00008
NM_006269.2(RP1):c.4131C>T (p.Asp1377=)	rs538825686	0.00007
NM_006269.2(RP1):c.4735T>G (p.Leu1579Val)	rs200860068	0.00005
NM_006269.2(RP1):c.6098G>A (p.Cys2033Tyr)	rs61739567

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