ClinVar Miner

List of variants in gene LOC122152296, USH2A studied for Retinitis pigmentosa 39

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_206933.4(USH2A):c.2633G>A (p.Arg878His) rs200124505 0.00011
NM_206933.4(USH2A):c.2414G>C (p.Gly805Ala) rs587783023 0.00009
NM_206933.4(USH2A):c.2802T>G (p.Cys934Trp) rs201527662 0.00006
NM_206933.4(USH2A):c.2792G>A (p.Cys931Tyr) rs145383772 0.00005
NM_206933.4(USH2A):c.2628T>A (p.Gly876=) rs768522338 0.00004
NM_206933.4(USH2A):c.2726C>A (p.Pro909His) rs752748453 0.00004
NM_206933.4(USH2A):c.2777G>A (p.Arg926His) rs146916397 0.00004
NM_206933.4(USH2A):c.2653C>T (p.His885Tyr) rs746071929 0.00002
NM_206933.4(USH2A):c.2479A>C (p.Asn827His) rs876658114 0.00001
NM_206933.4(USH2A):c.2541C>A (p.Cys847Ter) rs727503736 0.00001
NM_206933.4(USH2A):c.2610C>A (p.Cys870Ter) rs767078782 0.00001
NM_206933.4(USH2A):c.2617G>A (p.Gly873Arg) rs1037325220 0.00001
NM_206933.4(USH2A):c.2642A>C (p.Gln881Pro) rs769767476 0.00001
NM_206933.4(USH2A):c.2643G>A (p.Gln881=) rs1286317611 0.00001
NM_206933.4(USH2A):c.2761C>A (p.Leu921Met) rs772211390 0.00001
NM_206933.4(USH2A):c.2776C>T (p.Arg926Cys) rs749621457 0.00001
NM_206933.4(USH2A):c.2797C>T (p.Gln933Ter) rs1394737087 0.00001
NM_206933.4(USH2A):c.2309AAG[1] (p.Glu771del) rs1553320519
NM_206933.4(USH2A):c.2310dup (p.Glu771fs)
NM_206933.4(USH2A):c.2391_2392del (p.Cys797_Asp798delinsTer) rs2036063892
NM_206933.4(USH2A):c.2410C>T (p.Pro804Ser) rs2036063280
NM_206933.4(USH2A):c.2411del (p.Pro804fs)
NM_206933.4(USH2A):c.2431_2432del (p.Lys811fs) rs2102545818
NM_206933.4(USH2A):c.2440C>T (p.Gln814Ter)
NM_206933.4(USH2A):c.2525dup (p.Leu843fs) rs1403136669
NM_206933.4(USH2A):c.2615T>A (p.Leu872Ter)
NM_206933.4(USH2A):c.2616del (p.Gly873_Val874insTer) rs1553320451
NM_206933.4(USH2A):c.2647G>T (p.Glu883Ter)
NM_206933.4(USH2A):c.2649del (p.Glu883fs) rs2036054669
NM_206933.4(USH2A):c.2649dup (p.Pro884fs) rs2036054600
NM_206933.4(USH2A):c.2670del (p.Ile891fs)
NM_206933.4(USH2A):c.2691C>A (p.Cys897Ter)
NM_206933.4(USH2A):c.2692C>T (p.Gln898Ter)
NM_206933.4(USH2A):c.2710_2720dup (p.Leu908fs) rs755218835
NM_206933.4(USH2A):c.2750G>A (p.Ser917Asn) rs776323626
NM_206933.4(USH2A):c.2775T>C (p.Asn925=) rs779331611
NM_206933.4(USH2A):c.2779C>T (p.Gln927Ter) rs1438734382
NM_206933.4(USH2A):c.2809+1G>A rs759433119
NM_206933.4(USH2A):c.2809+1G>C rs759433119

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