ClinVar Miner

List of variants in gene CAPN3 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 72
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HGVS dbSNP gnomAD frequency
NM_000070.3(CAPN3):c.*134C>T rs3098423 0.97772
NM_000070.3(CAPN3):c.1116-226A>G rs3115877 0.93299
NM_000070.3(CAPN3):c.1992+110T>C rs3115883 0.77192
NM_000070.3(CAPN3):c.1783-893C>G rs2412711 0.76804
NM_000070.3(CAPN3):c.1537-48T>C rs2241827 0.76381
NM_000070.3(CAPN3):c.1915-298G>C rs3115882 0.61918
NM_000070.3(CAPN3):c.2381-79T>C rs3115884 0.44779
NM_000070.3(CAPN3):c.1782+183A>T rs7163986 0.27085
NM_000070.3(CAPN3):c.499-162T>C rs751572 0.24211
NM_000070.3(CAPN3):c.706G>A (p.Ala236Thr) rs1801449 0.23274
NM_000070.3(CAPN3):c.633-216C>T rs28364416 0.22506
NM_000070.3(CAPN3):c.310-244G>A rs28364388 0.15999
NM_000070.3(CAPN3):c.946-157C>G rs12324205 0.14423
NM_000070.3(CAPN3):c.1194-26C>G rs3743003 0.13055
NM_000070.3(CAPN3):c.633-69G>A rs4924675 0.12331
NM_000070.3(CAPN3):c.96T>C (p.Thr32=) rs1801496 0.09551
NM_000070.2(CAPN3):c.-408T>C rs16973174 0.09025
NM_000070.3(CAPN3):c.1193+163A>G rs3803342 0.07230
NM_000070.3(CAPN3):c.1746-221G>C rs28364498 0.07208
NM_000070.3(CAPN3):c.1783-59C>T rs28364508 0.07152
NM_000070.3(CAPN3):c.1800+143G>A rs28364509 0.06817
NM_000070.3(CAPN3):c.632+263A>G rs7174880 0.05652
NM_000070.3(CAPN3):c.1801-288G>C rs28364526 0.05301
NM_000070.3(CAPN3):c.606T>C (p.Ser202=) rs17593 0.05293
NM_000070.3(CAPN3):c.1536+133T>C rs28364491 0.05284
NM_000070.3(CAPN3):c.1914+30G>A rs2289293 0.05262
NM_000070.3(CAPN3):c.2381-114C>G rs28364541 0.05189
NM_000070.3(CAPN3):c.2381-132G>C rs28364540 0.05189
NM_000070.3(CAPN3):c.2439+69C>T rs28364544 0.05187
NM_000070.3(CAPN3):c.2380+12del rs28364538 0.04623
NM_000070.3(CAPN3):c.1029+3A>G rs28364442 0.03285
NM_000070.3(CAPN3):c.1116-116C>G rs16973233 0.03217
NM_000070.3(CAPN3):c.945+56C>T rs28364427 0.03098
NC_000015.10:g.42359484A>C rs28364363 0.03023
NM_000070.3(CAPN3):c.1915-98C>T rs28364532 0.02537
NM_000070.3(CAPN3):c.1783-63C>G rs28364507 0.02418
NM_000070.3(CAPN3):c.633-138C>T rs28364417 0.02383
NM_000070.3(CAPN3):c.802-120A>T rs28364426 0.02205
NM_000070.3(CAPN3):c.1536+263C>A rs28364493 0.02193
NM_000070.3(CAPN3):c.1800+150C>T rs28364510 0.02178
NM_000070.3(CAPN3):c.1354+61C>T rs28364474 0.01854
NM_000070.3(CAPN3):c.2116-186T>C rs28364534 0.01838
NM_000070.3(CAPN3):c.78G>A (p.Pro26=) rs62642519 0.01774
NM_000070.3(CAPN3):c.1992+42C>G rs8028539 0.01606
NM_000070.3(CAPN3):c.1030-164del rs201181640 0.01467
NM_000070.3(CAPN3):c.62G>A (p.Gly21Glu) rs28364364 0.01193
NM_000070.3(CAPN3):c.2433T>C (p.Val811=) rs28364543 0.01154
NM_000070.3(CAPN3):c.1116-5A>G rs28364467 0.01144
NM_000070.3(CAPN3):c.551C>T (p.Thr184Met) rs35889956 0.01026
NM_000070.3(CAPN3):c.2332G>A (p.Asp778Asn) rs115311625 0.00908
NM_000070.3(CAPN3):c.73C>T (p.His25Tyr) rs61735534 0.00885
NM_000070.3(CAPN3):c.319G>A (p.Glu107Lys) rs1801505 0.00719
NM_000070.3(CAPN3):c.939G>A (p.Pro313=) rs78369269 0.00698
NM_000070.3(CAPN3):c.984C>T (p.Cys328=) rs28364441 0.00600
NM_000070.3(CAPN3):c.2381-12A>G rs73402734 0.00578
NM_000070.3(CAPN3):c.1194-45C>T rs3743004 0.00414
NM_000070.3(CAPN3):c.1525-35del rs28364489 0.00243
NM_000070.3(CAPN3):c.309+12C>T rs200773265 0.00004
NM_000070.3(CAPN3):c.1030-104G>A rs28364454
NM_000070.3(CAPN3):c.1354+96G>A rs3743002
NM_000070.3(CAPN3):c.1355-154del rs35924291
NM_000070.3(CAPN3):c.1355-155_1355-154del rs35924291
NM_000070.3(CAPN3):c.1355-155_1355-154insTC rs3036710
NM_000070.3(CAPN3):c.1355-156C>T rs28364482
NM_000070.3(CAPN3):c.1355-156_1355-155insT rs531854862
NM_000070.3(CAPN3):c.1355-165C>G rs559361869
NM_000070.3(CAPN3):c.1782+263_1782+264insAGAG rs111814065
NM_000070.3(CAPN3):c.1783-781G>A rs28364503
NM_000070.3(CAPN3):c.2116-105G>C rs28364536
NM_000070.3(CAPN3):c.309+268dup rs397962506
NM_000070.3(CAPN3):c.632+217T>A rs28364410
NM_000070.3(CAPN3):c.802-221G>A rs2412709

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