ClinVar Miner

List of variants in gene RYR3 reported as likely benign by Invitae

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Total variants: 81
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HGVS dbSNP
NM_001036.4(RYR3):c.10113C>A (p.Leu3371=) rs770778818
NM_001036.4(RYR3):c.10503-6G>A rs183717988
NM_001036.4(RYR3):c.10503-7C>T rs374221046
NM_001036.4(RYR3):c.10674C>G (p.Leu3558=) rs765266347
NM_001036.4(RYR3):c.10788A>T (p.Glu3596Asp) rs200647737
NM_001036.4(RYR3):c.10806A>G (p.Lys3602=) rs118124507
NM_001036.4(RYR3):c.10816-9T>G rs10714306
NM_001036.4(RYR3):c.10959C>T (p.Ile3653=) rs367892350
NM_001036.4(RYR3):c.10971C>T (p.Asn3657=) rs371629185
NM_001036.4(RYR3):c.11067T>G (p.Ser3689=) rs201724283
NM_001036.4(RYR3):c.11397G>A (p.Gln3799=) rs373615131
NM_001036.4(RYR3):c.11514C>T (p.Asp3838=) rs371008125
NM_001036.4(RYR3):c.11859G>A (p.Gln3953=) rs189410371
NM_001036.4(RYR3):c.11876T>C (p.Ile3959Thr) rs114681942
NM_001036.4(RYR3):c.11931T>G (p.Val3977=) rs778575404
NM_001036.4(RYR3):c.12381G>A (p.Ala4127=) rs374756167
NM_001036.4(RYR3):c.13353C>G (p.Ser4451=) rs1555488276
NM_001036.4(RYR3):c.13569C>T (p.Thr4523=) rs759709172
NM_001036.4(RYR3):c.1373G>A (p.Arg458Gln) rs74005691
NM_001036.4(RYR3):c.147C>T (p.Phe49=) rs80182654
NM_001036.4(RYR3):c.1491C>T (p.Ser497=) rs746285785
NM_001036.4(RYR3):c.17A>G (p.Glu6Gly) rs562147027
NM_001036.4(RYR3):c.1922+9A>T rs760643042
NM_001036.4(RYR3):c.1953G>C (p.Ala651=) rs763470148
NM_001036.4(RYR3):c.2486G>A (p.Arg829His) rs199500216
NM_001036.4(RYR3):c.2532C>T (p.Leu844=) rs202183681
NM_001036.4(RYR3):c.2559C>T (p.Pro853=) rs189828361
NM_001036.4(RYR3):c.270C>T (p.Gly90=) rs372479066
NM_001036.4(RYR3):c.2770A>G (p.Thr924Ala) rs199638420
NM_001036.4(RYR3):c.3028-9G>A rs368914456
NM_001036.4(RYR3):c.3381+10T>C rs377602819
NM_001036.4(RYR3):c.348C>T (p.Ser116=) rs374563732
NM_001036.4(RYR3):c.3609C>T (p.Leu1203=) rs549685153
NM_001036.4(RYR3):c.363A>G (p.Thr121=) rs1555515067
NM_001036.4(RYR3):c.3954A>G (p.Gln1318=) rs372798643
NM_001036.4(RYR3):c.4165A>G (p.Met1389Val) rs542160399
NM_001036.4(RYR3):c.4380A>G (p.Glu1460=) rs201051485
NM_001036.4(RYR3):c.5256C>G (p.Pro1752=) rs1168377917
NM_001036.4(RYR3):c.5355C>T (p.Ala1785=) rs770898624
NM_001036.4(RYR3):c.5406C>T (p.Ser1802=) rs527977093
NM_001036.4(RYR3):c.5802C>A (p.Ile1934=) rs369574863
NM_001036.4(RYR3):c.5982G>A (p.Gly1994=) rs202185923
NM_001036.4(RYR3):c.5997G>A (p.Ala1999=) rs142550033
NM_001036.4(RYR3):c.6624G>A (p.Glu2208=) rs372003689
NM_001036.4(RYR3):c.6684C>T (p.Phe2228=) rs367645223
NM_001036.4(RYR3):c.6698G>A (p.Arg2233Gln) rs199648816
NM_001036.4(RYR3):c.6708G>A (p.Gly2236=) rs1485101035
NM_001036.4(RYR3):c.7089A>T (p.Ala2363=) rs1555429116
NM_001036.4(RYR3):c.725A>G (p.Asn242Ser) rs538703172
NM_001036.4(RYR3):c.7467C>T (p.Leu2489=) rs756348758
NM_001036.4(RYR3):c.7490A>G (p.Asn2497Ser) rs61996331
NM_001036.4(RYR3):c.7719G>A (p.Leu2573=) rs191980061
NM_001036.4(RYR3):c.7749A>G (p.Thr2583=) rs977035002
NM_001036.4(RYR3):c.7754C>G (p.Thr2585Arg) rs376084861
NM_001036.4(RYR3):c.7812C>G (p.Asn2604Lys) rs41279214
NM_001036.4(RYR3):c.7848C>T (p.Tyr2616=) rs7165225
NM_001036.4(RYR3):c.789T>G (p.Leu263=) rs758671481
NM_001036.4(RYR3):c.8016G>A (p.Ala2672=) rs201746379
NM_001036.4(RYR3):c.8516-5C>T rs111370716
NM_001036.4(RYR3):c.8516-8C>T rs763876855
NM_001036.4(RYR3):c.8542G>A (p.Glu2848Lys) rs190035689
NM_001036.4(RYR3):c.8667C>T (p.Ser2889=) rs201031443
NM_001036.4(RYR3):c.8703C>T (p.Ala2901=) rs186614396
NM_001036.4(RYR3):c.8724C>T (p.Ala2908=) rs199745365
NM_001036.4(RYR3):c.8748C>T (p.Ser2916=) rs762140107
NM_001036.4(RYR3):c.8755+9A>G rs748002152
NM_001036.4(RYR3):c.8865A>C (p.Ala2955=) rs1555450889
NM_001036.4(RYR3):c.8914A>G (p.Lys2972Glu) rs201961808
NM_001036.4(RYR3):c.8943G>A (p.Thr2981=) rs1002586633
NM_001036.4(RYR3):c.8956G>A (p.Val2986Ile) rs189282419
NM_001036.4(RYR3):c.8984T>A (p.Val2995Glu) rs192484612
NM_001036.4(RYR3):c.9006G>A (p.Thr3002=) rs200133020
NM_001036.4(RYR3):c.9225T>C (p.Asn3075=) rs753270695
NM_001036.4(RYR3):c.9268+8T>C rs369156367
NM_001036.4(RYR3):c.9354C>T (p.Ala3118=) rs759031318
NM_001036.4(RYR3):c.9355G>A (p.Glu3119Lys) rs200830195
NM_001036.4(RYR3):c.9589+5C>T rs73383308
NM_001036.4(RYR3):c.9589+6G>A rs575029619
NM_001036.4(RYR3):c.9590-4G>A rs376097393
NM_001036.4(RYR3):c.9799C>T (p.Pro3267Ser) rs182972491
NM_001036.4(RYR3):c.9950T>C (p.Ile3317Thr) rs150028316

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