ClinVar Miner

List of variants in gene RYR3 reported as benign by Invitae

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Total variants: 75
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HGVS dbSNP
NM_001036.4(RYR3):c.52-8_52-6delCCT rs138901366
NM_001036.5(RYR3):c.10278A>G (p.Lys3426=) rs16958093
NM_001036.5(RYR3):c.10569C>A (p.Ser3523=) rs747519835
NM_001036.5(RYR3):c.10698G>A (p.Thr3566=) rs200309704
NM_001036.5(RYR3):c.10719C>T (p.Asp3573=) rs58745096
NM_001036.5(RYR3):c.1073T>C (p.Ile358Thr) rs2304380
NM_001036.5(RYR3):c.10816-9T>C rs10714306
NM_001036.5(RYR3):c.10921A>G (p.Met3641Val) rs146201205
NM_001036.5(RYR3):c.11073-8A>G rs8029260
NM_001036.5(RYR3):c.1110C>T (p.Asp370=) rs16972317
NM_001036.5(RYR3):c.11196G>A (p.Thr3732=) rs148918638
NM_001036.5(RYR3):c.11289C>T (p.Thr3763=) rs138744371
NM_001036.5(RYR3):c.11464-8C>A rs200401387
NM_001036.5(RYR3):c.11545A>C (p.Asn3849His) rs202181075
NM_001036.5(RYR3):c.12129T>C (p.Arg4043=) rs115338509
NM_001036.5(RYR3):c.12516G>C (p.Val4172=) rs75286462
NM_001036.5(RYR3):c.12558C>G (p.Ser4186=) rs73372074
NM_001036.5(RYR3):c.1277A>G (p.Asn426Ser) rs146838868
NM_001036.5(RYR3):c.1295T>G (p.Ile432Ser) rs202244063
NM_001036.5(RYR3):c.13151C>T (p.Pro4384Leu) rs200281542
NM_001036.5(RYR3):c.13168A>G (p.Asn4390Asp) rs142108245
NM_001036.5(RYR3):c.13365G>A (p.Glu4455=) rs118177681
NM_001036.5(RYR3):c.13497+6C>T rs116123066
NM_001036.5(RYR3):c.1437+8G>A rs190742260
NM_001036.5(RYR3):c.1788+10G>C rs146892882
NM_001036.5(RYR3):c.1828G>A (p.Val610Ile) rs114825824
NM_001036.5(RYR3):c.2164+8C>T rs75782410
NM_001036.5(RYR3):c.2214G>A (p.Ser738=) rs201215774
NM_001036.5(RYR3):c.2502T>A (p.Ile834=) rs2229118
NM_001036.5(RYR3):c.2574+3A>C rs182429820
NM_001036.5(RYR3):c.2693A>G (p.Asn898Ser) rs2229119
NM_001036.5(RYR3):c.2784-10T>G rs565033705
NM_001036.5(RYR3):c.280-7C>G rs2304386
NM_001036.5(RYR3):c.3557-7T>G rs183792071
NM_001036.5(RYR3):c.4396-10C>T rs78825800
NM_001036.5(RYR3):c.4468C>T (p.Leu1490=) rs74005937
NM_001036.5(RYR3):c.4473C>T (p.Asp1491=) rs61996324
NM_001036.5(RYR3):c.4611C>T (p.Pro1537=) rs61996325
NM_001036.5(RYR3):c.4701G>A (p.Ala1567=) rs115119086
NM_001036.5(RYR3):c.4821T>C (p.Tyr1607=) rs200740143
NM_001036.5(RYR3):c.5033A>G (p.Asp1678Gly) rs59021219
NM_001036.5(RYR3):c.5299G>A (p.Glu1767Lys) rs115321092
NM_001036.5(RYR3):c.5419-8C>G rs183255287
NM_001036.5(RYR3):c.5484A>G (p.Ala1828=) rs187371252
NM_001036.5(RYR3):c.5620-5C>G rs80354707
NM_001036.5(RYR3):c.5959C>A (p.Arg1987=) rs187374038
NM_001036.5(RYR3):c.6125A>G (p.Asn2042Ser) rs116926961
NM_001036.5(RYR3):c.6134+9T>C rs113699058
NM_001036.5(RYR3):c.6444T>C (p.Asn2148=) rs61996329
NM_001036.5(RYR3):c.6617A>C (p.Asn2206Thr) rs181264765
NM_001036.5(RYR3):c.6960G>C (p.Leu2320=) rs139287308
NM_001036.5(RYR3):c.7062G>A (p.Ala2354=) rs74005974
NM_001036.5(RYR3):c.7516-8C>T rs74005978
NM_001036.5(RYR3):c.7581C>T (p.Tyr2527=) rs112521485
NM_001036.5(RYR3):c.7632G>T (p.Gly2544=) rs115185294
NM_001036.5(RYR3):c.7689G>A (p.Leu2563=) rs186300217
NM_001036.5(RYR3):c.7827C>G (p.Ser2609=) rs149242033
NM_001036.5(RYR3):c.78C>A (p.Ile26=) rs199968653
NM_001036.5(RYR3):c.8117G>T (p.Ser2706Ile) rs201561672
NM_001036.5(RYR3):c.8136+9C>G rs41279216
NM_001036.5(RYR3):c.8400-5C>T rs74437672
NM_001036.5(RYR3):c.8481C>T (p.Tyr2827=) rs188257094
NM_001036.5(RYR3):c.8555G>A (p.Arg2852His) rs150799181
NM_001036.5(RYR3):c.855A>T (p.Arg285=) rs41279202
NM_001036.5(RYR3):c.8641T>A (p.Ser2881Thr) rs61996340
NM_001036.5(RYR3):c.8997C>T (p.Pro2999=) rs8041960
NM_001036.5(RYR3):c.8997_8998inv (p.Ile3000Val)
NM_001036.5(RYR3):c.8998A>G (p.Ile3000Val) rs10851894
NM_001036.5(RYR3):c.9143G>T (p.Arg3048Leu) rs139568967
NM_001036.5(RYR3):c.9254C>G (p.Pro3085Arg) rs61996335
NM_001036.5(RYR3):c.9686C>T (p.Thr3229Met) rs61996338
NM_001036.5(RYR3):c.9759C>T (p.Asp3253=) rs55650127
NM_001036.5(RYR3):c.9816C>T (p.Tyr3272=) rs61996336
NM_001036.5(RYR3):c.9831-8G>C rs377437662
NM_001036.5(RYR3):c.9873C>G (p.Leu3291=) rs147149598

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