ClinVar Miner

List of variants in gene RYR3 reported as likely benign for not provided

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Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_001036.6(RYR3):c.9759C>T (p.Asp3253=) rs55650127 0.00531
NM_001036.6(RYR3):c.8705+17A>C rs148404688 0.00508
NM_001036.6(RYR3):c.11289C>T (p.Thr3763=) rs138744371 0.00493
NM_001036.6(RYR3):c.9254C>G (p.Pro3085Arg) rs61996335 0.00307
NM_001036.6(RYR3):c.4701G>A (p.Ala1567=) rs115119086 0.00288
NM_001036.6(RYR3):c.8555G>A (p.Arg2852His) rs150799181 0.00265
NM_001036.6(RYR3):c.4473C>T (p.Asp1491=) rs61996324 0.00260
NM_001036.6(RYR3):c.9873C>G (p.Leu3291=) rs147149598 0.00253
NM_001036.6(RYR3):c.7812C>G (p.Asn2604Lys) rs41279214 0.00237
NM_001036.6(RYR3):c.9355G>A (p.Glu3119Lys) rs200830195 0.00200
NM_001036.6(RYR3):c.4821T>C (p.Tyr1607=) rs200740143 0.00180
NM_001036.6(RYR3):c.10921A>G (p.Met3641Val) rs146201205 0.00168
NM_001036.6(RYR3):c.10698G>A (p.Thr3566=) rs200309704 0.00163
NM_001036.6(RYR3):c.11196G>A (p.Thr3732=) rs148918638 0.00155
NM_001036.6(RYR3):c.11464-8C>A rs200401387 0.00152
NM_001036.6(RYR3):c.9950T>C (p.Ile3317Thr) rs150028316 0.00149
NM_001036.6(RYR3):c.7827C>G (p.Ser2609=) rs149242033 0.00139
NM_001036.6(RYR3):c.2486G>A (p.Arg829His) rs199500216 0.00128
NM_001036.6(RYR3):c.5484A>G (p.Ala1828=) rs187371252 0.00127
NM_001036.6(RYR3):c.2214G>A (p.Ser738=) rs201215774 0.00105
NM_001036.6(RYR3):c.1373G>A (p.Arg458Gln) rs74005691 0.00083
NM_001036.6(RYR3):c.8703C>T (p.Ala2901=) rs186614396 0.00071
NM_001036.6(RYR3):c.8481C>T (p.Tyr2827=) rs188257094 0.00068
NM_001036.6(RYR3):c.621G>A (p.Thr207=) rs370200639 0.00048
NM_001036.6(RYR3):c.8016G>A (p.Ala2672=) rs201746379 0.00039
NM_001036.6(RYR3):c.10971C>T (p.Asn3657=) rs371629185 0.00033
NM_001036.6(RYR3):c.348C>T (p.Ser116=) rs374563732 0.00010
NM_001036.6(RYR3):c.10743C>G (p.Ser3581=) rs778205832 0.00009
NM_001036.6(RYR3):c.288A>G (p.Gln96=) rs760794454 0.00009
NM_001036.6(RYR3):c.7754C>G (p.Thr2585Arg) rs376084861 0.00006
NM_001036.6(RYR3):c.1911C>T (p.Asn637=) rs199980142 0.00005
NM_001036.6(RYR3):c.12979-6G>T rs191896519 0.00003
NM_001036.6(RYR3):c.6966C>T (p.Ser2322=) rs374683480 0.00003
NM_001036.6(RYR3):c.7113C>T (p.Arg2371=) rs751258576 0.00003
NM_001036.6(RYR3):c.10731C>T (p.Tyr3577=) rs1029342661 0.00001
NM_001036.6(RYR3):c.3176-10C>T rs1168419982 0.00001
NM_001036.6(RYR3):c.3177T>G (p.Ala1059=) rs1595911537 0.00001
NM_001036.6(RYR3):c.4989C>T (p.Pro1663=) rs768997188 0.00001
NM_001036.6(RYR3):c.5217T>C (p.Asp1739=) rs1039031106 0.00001
NM_001036.6(RYR3):c.6390G>A (p.Ser2130=) rs187165112 0.00001
NM_001036.6(RYR3):c.7248T>C (p.Tyr2416=) rs201117522 0.00001
GRCh37/hg19 15q14(chr15:33676561-33707835)x1
NM_001036.6(RYR3):c.10503-1446_10503-1445del
NM_001036.6(RYR3):c.1209G>A (p.Glu403=) rs1595624306
NM_001036.6(RYR3):c.12909C>G (p.Leu4303=)
NM_001036.6(RYR3):c.1437+7C>T rs748318941
NM_001036.6(RYR3):c.15A>G (p.Gly5=) rs1453652852
NM_001036.6(RYR3):c.1812C>T (p.Leu604=)
NM_001036.6(RYR3):c.234C>A (p.Ala78=) rs776514533
NM_001036.6(RYR3):c.2433A>G (p.Glu811=) rs1595874286
NM_001036.6(RYR3):c.2790C>T (p.Leu930=)
NM_001036.6(RYR3):c.282A>G (p.Ala94=) rs764425213
NM_001036.6(RYR3):c.2883C>T (p.Asn961=)
NM_001036.6(RYR3):c.3176-5A>T rs1403323558
NM_001036.6(RYR3):c.3933C>T (p.Phe1311=) rs1595957571
NM_001036.6(RYR3):c.5076G>A (p.Arg1692=)
NM_001036.6(RYR3):c.5355C>A (p.Ala1785=) rs770898624
NM_001036.6(RYR3):c.6125A>G (p.Asn2042Ser) rs116926961
NM_001036.6(RYR3):c.6894C>T (p.Arg2298=) rs1596317090
NM_001036.6(RYR3):c.7272C>T (p.Leu2424=)
NM_001036.6(RYR3):c.7820+7C>A rs749413810
NM_001036.6(RYR3):c.8756-8T>A rs1453242045

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