ClinVar Miner

List of variants in gene RP1 reported as benign

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Gene type:
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Total variants: 36
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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.4565G>A (p.Gly1522Asp) rs77860871 0.00580
NM_006269.2(RP1):c.885T>C (p.Val295=) rs80043423 0.00468
NM_006269.2(RP1):c.616-6T>C rs186571865 0.00458
NM_006269.2(RP1):c.382C>A (p.Leu128Ile) rs147116231 0.00283
NM_006269.2(RP1):c.279G>T (p.Thr93=) rs144293929 0.00184
NM_006269.2(RP1):c.4509T>C (p.Thr1503=) rs144274712 0.00151
NM_006269.2(RP1):c.4512A>G (p.Leu1504=) rs148722424 0.00150
NM_006269.2(RP1):c.6366T>C (p.Ile2122=) rs114157620 0.00144
NM_006269.2(RP1):c.4511T>C (p.Leu1504Ser) rs138106612 0.00127
NM_006269.2(RP1):c.2385C>T (p.Ile795=) rs184739468 0.00105
NM_006269.2(RP1):c.487G>A (p.Asp163Asn) rs370436803 0.00074
NM_006269.2(RP1):c.228C>T (p.Leu76=) rs142600056 0.00073
NM_006269.2(RP1):c.618T>C (p.Val206=) rs146337514 0.00051
NM_006269.2(RP1):c.*71C>T rs185876566 0.00028
NM_006269.2(RP1):c.2116G>C (p.Gly706Arg) rs199879316 0.00014
NM_006269.2(RP1):c.2938G>A (p.Gly980Ser) rs202226256 0.00014
NM_006269.2(RP1):c.4299A>G (p.Ala1433=) rs148918111 0.00013
NM_006269.2(RP1):c.441C>T (p.Pro147=) rs547844896 0.00012
NM_006269.2(RP1):c.2894G>T (p.Ser965Ile) rs201110322 0.00009
NM_006269.2(RP1):c.3024G>A (p.Gln1008=) rs555160408 0.00009
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_001375654.1(RP1):c.1205A>T (p.Glu402Val)
NM_001375654.1(RP1):c.1459T>C (p.Tyr487His)
NM_006269.2(RP1):c.4876G>A (p.Gly1626Arg) rs527236106
NM_006269.2(RP1):c.6098G>A (p.Cys2033Tyr) rs61739567

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