ClinVar Miner

List of variants in gene SUCLA2 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_003850.3(SUCLA2):c.534+104A>G rs115177648 0.02847
NM_003850.3(SUCLA2):c.1107+278G>A rs77175891 0.02739
NM_003850.3(SUCLA2):c.1108-258G>A rs114659630 0.02643
NM_003850.3(SUCLA2):c.1108-59T>G rs41284201 0.01288
NM_003850.3(SUCLA2):c.535-116A>G rs148740101 0.01261
NM_003850.3(SUCLA2):c.664-189A>G rs79358571 0.01217
NM_003850.3(SUCLA2):c.271+146T>C rs77027862 0.00922
NM_003850.3(SUCLA2):c.1229-124T>C rs116556378 0.00739
NC_000013.11:g.48001481dup rs144202274 0.00636
NM_003850.3(SUCLA2):c.534+106T>C rs116245479 0.00577
NM_003850.3(SUCLA2):c.91-267G>A rs115546815 0.00465
NM_003850.3(SUCLA2):c.272-140G>A rs182987275 0.00461
NM_003850.3(SUCLA2):c.663+324C>T rs189551270 0.00439
NM_003850.3(SUCLA2):c.802+84A>C rs138767248 0.00416
NM_003850.3(SUCLA2):c.*132A>G rs115959143 0.00362
NM_003850.3(SUCLA2):c.271+35A>G rs186142828 0.00354
NM_003850.3(SUCLA2):c.660C>T (p.Leu220=) rs148794726 0.00051
NM_003850.3(SUCLA2):c.372-6T>C rs139004670 0.00046
NM_003850.3(SUCLA2):c.1350G>A (p.Ala450=) rs144969057 0.00036
NM_003850.3(SUCLA2):c.1108-45T>G rs146144810 0.00032
NM_003850.3(SUCLA2):c.942C>T (p.Leu314=) rs368442407 0.00016
NM_003850.3(SUCLA2):c.21C>T (p.Tyr7=) rs374479008 0.00014
NM_003850.3(SUCLA2):c.9C>T (p.Ala3=) rs138270687 0.00013
NM_003850.3(SUCLA2):c.268T>A (p.Leu90Ile) rs149929505 0.00007
NM_003850.3(SUCLA2):c.210C>T (p.Ser70=) rs1203177405 0.00001
NM_003850.3(SUCLA2):c.916A>C (p.Lys306Gln) rs775767182 0.00001
NM_003850.3(SUCLA2):c.964+17T>C rs779776982 0.00001
NM_003850.2(SUCLA2):c.-12T>A rs753085253
NM_003850.3(SUCLA2):c.1317+188C>T rs115548571
NM_003850.3(SUCLA2):c.1353G>A (p.Lys451=) rs754141542
NM_003850.3(SUCLA2):c.219A>C (p.Lys73Asn) rs796052043
NM_003850.3(SUCLA2):c.272-247_272-246dup rs11445752
NM_003850.3(SUCLA2):c.390T>C (p.Ala130=) rs1555259469
NM_003850.3(SUCLA2):c.490A>C (p.Arg164=) rs745493625
NM_003850.3(SUCLA2):c.534+27C>T rs187268157
NM_003850.3(SUCLA2):c.664-159_664-156del rs147091118
NM_003850.3(SUCLA2):c.688C>T (p.Pro230Ser) rs796052047

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