ClinVar Miner

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

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Gene type:
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Total variants: 89
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HGVS dbSNP
NM_001036.5(RYR3):c.10113C>A (p.Leu3371=) rs770778818
NM_001036.5(RYR3):c.10389+10A>G rs1346473227
NM_001036.5(RYR3):c.10731C>T (p.Tyr3577=) rs1029342661
NM_001036.5(RYR3):c.10816-9T>G rs10714306
NM_001036.5(RYR3):c.10816-9_10816-8del rs1596804345
NM_001036.5(RYR3):c.11147-7T>C rs1596837665
NM_001036.5(RYR3):c.11147-8A>G rs776534103
NM_001036.5(RYR3):c.1209G>A (p.Glu403=) rs1595624306
NM_001036.5(RYR3):c.12642G>A (p.Val4214=) rs1201772266
NM_001036.5(RYR3):c.12810G>T (p.Gly4270=) rs778158975
NM_001036.5(RYR3):c.12979-6G>T rs191896519
NM_001036.5(RYR3):c.13071A>G (p.Lys4357=) rs748419368
NM_001036.5(RYR3):c.1329A>G (p.Leu443=) rs1278028525
NM_001036.5(RYR3):c.13353C>G (p.Ser4451=) rs1555488276
NM_001036.5(RYR3):c.13437C>T (p.Ala4479=) rs377281161
NM_001036.5(RYR3):c.1437+7C>T rs748318941
NM_001036.5(RYR3):c.15A>G (p.Gly5=) rs1453652852
NM_001036.5(RYR3):c.1737C>T (p.Gly579=) rs369591701
NM_001036.5(RYR3):c.17A>G (p.Glu6Gly) rs562147027
NM_001036.5(RYR3):c.1911C>T (p.Asn637=) rs199980142
NM_001036.5(RYR3):c.1950C>T (p.Val650=) rs763303513
NM_001036.5(RYR3):c.1953G>C (p.Ala651=) rs763470148
NM_001036.5(RYR3):c.2094A>G (p.Glu698=) rs1595791362
NM_001036.5(RYR3):c.234C>A (p.Ala78=) rs776514533
NM_001036.5(RYR3):c.2433A>G (p.Glu811=) rs1595874286
NM_001036.5(RYR3):c.282A>G (p.Ala94=) rs764425213
NM_001036.5(RYR3):c.2910G>A (p.Leu970=) rs541322440
NM_001036.5(RYR3):c.2931T>A (p.Pro977=) rs1595902112
NM_001036.5(RYR3):c.2964A>G (p.Glu988=) rs1595902210
NM_001036.5(RYR3):c.3028-10C>T rs374572025
NM_001036.5(RYR3):c.3070T>C (p.Leu1024=) rs752015882
NM_001036.5(RYR3):c.315C>T (p.Tyr105=) rs537373426
NM_001036.5(RYR3):c.3176-10C>T rs1168419982
NM_001036.5(RYR3):c.3176-5A>T rs1403323558
NM_001036.5(RYR3):c.3177T>G (p.Ala1059=) rs1595911537
NM_001036.5(RYR3):c.3214C>A (p.Arg1072=) rs764599185
NM_001036.5(RYR3):c.3303C>T (p.Val1101=) rs752550511
NM_001036.5(RYR3):c.3627C>G (p.Thr1209=) rs372693148
NM_001036.5(RYR3):c.3738C>T (p.Asn1246=) rs372929421
NM_001036.5(RYR3):c.3816G>A (p.Thr1272=) rs770156777
NM_001036.5(RYR3):c.3882C>T (p.Val1294=) rs779754319
NM_001036.5(RYR3):c.3903C>T (p.Ser1301=) rs1595957366
NM_001036.5(RYR3):c.3933C>T (p.Phe1311=) rs1595957571
NM_001036.5(RYR3):c.4476C>G (p.Val1492=) rs1596022012
NM_001036.5(RYR3):c.4677C>T (p.Tyr1559=) rs756679547
NM_001036.5(RYR3):c.4683G>A (p.Thr1561=) rs771772947
NM_001036.5(RYR3):c.46A>C (p.Arg16=) rs1595668424
NM_001036.5(RYR3):c.4989C>T (p.Pro1663=) rs768997188
NM_001036.5(RYR3):c.51+9C>T rs1595668505
NM_001036.5(RYR3):c.5217T>C (p.Asp1739=) rs1039031106
NM_001036.5(RYR3):c.5355C>T (p.Ala1785=) rs770898624
NM_001036.5(RYR3):c.5413C>T (p.Leu1805=) rs747408262
NM_001036.5(RYR3):c.5419-9T>A rs372099114
NM_001036.5(RYR3):c.552C>G (p.Leu184=) rs1595509178
NM_001036.5(RYR3):c.5802C>A (p.Ile1934=) rs369574863
NM_001036.5(RYR3):c.5889G>A (p.Thr1963=) rs1281447838
NM_001036.5(RYR3):c.6125A>C (p.Asn2042Thr) rs116926961
NM_001036.5(RYR3):c.6125A>G (p.Asn2042Ser) rs116926961
NM_001036.5(RYR3):c.6135-4C>G rs763332893
NM_001036.5(RYR3):c.6483+7G>A rs768641537
NM_001036.5(RYR3):c.6525C>T (p.Pro2175=) rs1596258502
NM_001036.5(RYR3):c.6690G>A (p.Pro2230=) rs757123345
NM_001036.5(RYR3):c.6800+9A>T rs1596313377
NM_001036.5(RYR3):c.6886C>T (p.Leu2296=) rs1204903519
NM_001036.5(RYR3):c.6891C>T (p.Gly2297=) rs754179311
NM_001036.5(RYR3):c.6894C>T (p.Arg2298=) rs1596317090
NM_001036.5(RYR3):c.6966C>T (p.Ser2322=) rs374683480
NM_001036.5(RYR3):c.7113C>T (p.Arg2371=) rs751258576
NM_001036.5(RYR3):c.7158G>A (p.Glu2386=) rs749172404
NM_001036.5(RYR3):c.7248T>C (p.Tyr2416=) rs201117522
NM_001036.5(RYR3):c.7341G>A (p.Gln2447=) rs1596343898
NM_001036.5(RYR3):c.7350C>T (p.Tyr2450=) rs1452135793
NM_001036.5(RYR3):c.7644G>A (p.Ser2548=) rs763362837
NM_001036.5(RYR3):c.7820+7C>A rs749413810
NM_001036.5(RYR3):c.7890C>T (p.Ala2630=) rs58775107
NM_001036.5(RYR3):c.789T>G (p.Leu263=) rs758671481
NM_001036.5(RYR3):c.8026C>T (p.Leu2676=) rs767902428
NM_001036.5(RYR3):c.8200-7del rs1596418008
NM_001036.5(RYR3):c.8244C>G (p.Ala2748=) rs1033099305
NM_001036.5(RYR3):c.8667C>T (p.Ser2889=) rs201031443
NM_001036.5(RYR3):c.8705+17A>C rs148404688
NM_001036.5(RYR3):c.8756-8T>A rs1453242045
NM_001036.5(RYR3):c.9056-7G>A rs770665101
NM_001036.5(RYR3):c.9105C>T (p.Ser3035=) rs1596526066
NM_001036.5(RYR3):c.9129T>C (p.Tyr3043=) rs1250990985
NM_001036.5(RYR3):c.9225T>C (p.Asn3075=) rs753270695
NM_001036.5(RYR3):c.9477A>G (p.Pro3159=) rs765087383
NM_001036.5(RYR3):c.9705G>A (p.Gln3235=) rs1596588961
NM_001036.5(RYR3):c.973-1G>C rs552370646

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