ClinVar Miner

List of variants in gene CAPN3 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP
NC_000015.10:g.42359398T>C
NM_000070.3(CAPN3):c.1029+3A>G rs28364442
NM_000070.3(CAPN3):c.1116-116C>G
NM_000070.3(CAPN3):c.1116-226A>G
NM_000070.3(CAPN3):c.1116-5A>G rs28364467
NM_000070.3(CAPN3):c.1194-26C>G rs3743003
NM_000070.3(CAPN3):c.1194-45C>T rs3743004
NM_000070.3(CAPN3):c.1355-6G>A rs28364485
NM_000070.3(CAPN3):c.1537-48T>C rs2241827
NM_000070.3(CAPN3):c.1782+183A>T
NM_000070.3(CAPN3):c.1782+263_1782+264insAGAG
NM_000070.3(CAPN3):c.1783-893C>G
NM_000070.3(CAPN3):c.1915-298G>C
NM_000070.3(CAPN3):c.1992+110T>C
NM_000070.3(CAPN3):c.2332G>A (p.Asp778Asn) rs115311625
NM_000070.3(CAPN3):c.2380+12del rs28364538
NM_000070.3(CAPN3):c.2381-12A>G rs73402734
NM_000070.3(CAPN3):c.2381-79T>C
NM_000070.3(CAPN3):c.2433T>C (p.Val811=) rs28364543
NM_000070.3(CAPN3):c.309+12C>T rs200773265
NM_000070.3(CAPN3):c.310-244G>A
NM_000070.3(CAPN3):c.319G>A (p.Glu107Lys) rs1801505
NM_000070.3(CAPN3):c.479C>G (p.Ala160Gly) rs17592
NM_000070.3(CAPN3):c.495C>T (p.Phe165=) rs1801324
NM_000070.3(CAPN3):c.498+126A>G
NM_000070.3(CAPN3):c.498+329G>A
NM_000070.3(CAPN3):c.498+35G>T rs28364399
NM_000070.3(CAPN3):c.499-162T>C
NM_000070.3(CAPN3):c.551C>T (p.Thr184Met) rs35889956
NM_000070.3(CAPN3):c.606T>C (p.Ser202=) rs17593
NM_000070.3(CAPN3):c.62G>A (p.Gly21Glu) rs28364364
NM_000070.3(CAPN3):c.632+263A>G
NM_000070.3(CAPN3):c.633-216C>T
NM_000070.3(CAPN3):c.706G>A (p.Ala236Thr) rs1801449
NM_000070.3(CAPN3):c.73C>T (p.His25Tyr) rs61735534
NM_000070.3(CAPN3):c.78G>A (p.Pro26=) rs62642519
NM_000070.3(CAPN3):c.939G>A (p.Pro313=) rs78369269
NM_000070.3(CAPN3):c.946-157C>G
NM_000070.3(CAPN3):c.96T>C (p.Thr32=) rs1801496
NM_000070.3(CAPN3):c.984C>T (p.Cys328=) rs28364441

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