ClinVar Miner

List of variants in gene CARS2 reported as likely benign by GeneDx

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Gene type:
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Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_024537.4(CARS2):c.786-125T>C rs76243178 0.01838
NM_024537.4(CARS2):c.656-205T>G rs80279244 0.01678
NM_024537.4(CARS2):c.1054+188G>C rs116168677 0.01599
NM_024537.4(CARS2):c.1317+27G>A rs116312064 0.01281
NM_024537.4(CARS2):c.1318-142C>T rs114776169 0.01263
NM_024537.4(CARS2):c.1317+24T>C rs114840063 0.01047
NM_024537.4(CARS2):c.571+334G>A rs115225996 0.00665
NM_024537.4(CARS2):c.655+283T>G rs115504252 0.00660
NM_024537.4(CARS2):c.1054+8G>A rs374859 0.00434
NM_024537.4(CARS2):c.1417-17C>T rs113709957 0.00417
NM_024537.4(CARS2):c.920-169C>T rs141762931 0.00404
NM_024537.4(CARS2):c.1623+59G>A rs148358273 0.00391
NM_024537.4(CARS2):c.1193+25C>T rs185149092 0.00364
NM_024537.4(CARS2):c.1193+230G>C rs7322137 0.00361
NM_024537.4(CARS2):c.1128C>T (p.Asp376=) rs142070578 0.00308
NM_024537.4(CARS2):c.1632C>A (p.Ser544Arg) rs141184379 0.00297
NM_024537.4(CARS2):c.276-47T>C rs114897295 0.00252
NM_024537.4(CARS2):c.930C>T (p.His310=) rs143532600 0.00232
NM_024537.4(CARS2):c.1054+41G>A rs192671914 0.00228
NM_024537.4(CARS2):c.1531G>A (p.Ala511Thr) rs147216443 0.00166
NM_024537.4(CARS2):c.1318-12G>A rs191969046 0.00161
NM_024537.4(CARS2):c.465+14C>T rs41315944 0.00061
NM_024537.4(CARS2):c.244G>A (p.Val82Ile) rs117788141 0.00055
NM_024537.4(CARS2):c.564G>A (p.Thr188=) rs76988055 0.00049
NM_024537.4(CARS2):c.1287C>T (p.His429=) rs143945861 0.00041
NM_024537.4(CARS2):c.1318-18C>T rs185912329 0.00034
NM_024537.4(CARS2):c.571+11T>C rs373960867 0.00031
NM_024537.4(CARS2):c.1308G>A (p.Ala436=) rs141349632 0.00027
NM_024537.4(CARS2):c.1074C>T (p.Ser358=) rs143638615 0.00025
NM_024537.4(CARS2):c.741A>T (p.Gly247=) rs998783511 0.00016
NM_024537.4(CARS2):c.466-18G>A rs370423607 0.00013
NM_024537.4(CARS2):c.1194-17C>G rs377292484 0.00009
NM_024537.4(CARS2):c.1503G>A (p.Ala501=) rs753425826 0.00007
NM_024537.4(CARS2):c.1608C>T (p.His536=) rs748996703 0.00005
NM_024537.4(CARS2):c.1011C>T (p.Pro337=) rs142857490 0.00004
NM_024537.4(CARS2):c.1407A>C (p.Ala469=) rs780686611 0.00004
NM_024537.4(CARS2):c.1647G>A (p.Thr549=) rs201728933 0.00004
NM_024537.4(CARS2):c.528T>C (p.Ile176=) rs759194567 0.00003
NM_024537.4(CARS2):c.920-18C>A rs1057521365 0.00003
NM_024537.4(CARS2):c.1689G>A (p.Ala563=) rs774357584 0.00002
NM_024537.4(CARS2):c.855C>T (p.Asn285=) rs201463850 0.00002
NM_024537.4(CARS2):c.1008C>T (p.Ser336=) rs1313306865 0.00001
NM_024537.4(CARS2):c.1257G>A (p.Val419=) rs774758878 0.00001
NM_024537.4(CARS2):c.1473G>A (p.Val491=) rs774705663 0.00001
NM_024537.4(CARS2):c.744C>T (p.Pro248=) rs747726067 0.00001
NM_024537.4(CARS2):c.1623+17G>A rs550431344
NM_024537.4(CARS2):c.1624-299_1624-295del rs367742376
NM_024537.4(CARS2):c.394-13A>C rs575543110
NM_024537.4(CARS2):c.920-18C>T rs1057521365

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