List of variants in gene CARS2 reported as likely benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

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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.1624-12C>G	rs115116722	0.00724
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.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.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.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.1167C>T (p.Ser389=)	rs41275134	0.00006
NM_024537.4(CARS2):c.1011C>T (p.Pro337=)	rs142857490	0.00004
NM_024537.4(CARS2):c.1647G>A (p.Thr549=)	rs201728933	0.00004
NM_024537.4(CARS2):c.1624-299_1624-295del	rs367742376
NM_024537.4(CARS2):c.1683dup (p.Ser562fs)	rs575601185
NM_024537.4(CARS2):c.279A>T (p.Ser93=)	rs1223903959
NM_024537.4(CARS2):c.394-13A>C	rs575543110

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