List of variants in gene SLC3A1 reported as benign for Cystinuria

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_000341.4(SLC3A1):c.114A>C (p.Gly38=)	rs3738985	0.75388
NM_000341.4(SLC3A1):c.1332+7C>T	rs3738984	0.61143
NM_000341.4(SLC3A1):c.892-6C>G	rs114640930	0.00594
NM_000341.4(SLC3A1):c.1572C>T (p.Asn524=)	rs149590349	0.00368
NM_000341.4(SLC3A1):c.300C>T (p.Leu100=)	rs115030299	0.00351
NM_000341.4(SLC3A1):c.1035G>A (p.Glu345=)	rs78795495	0.00338
NM_000341.4(SLC3A1):c.1012-23C>T	rs201121824	0.00284
NM_000341.4(SLC3A1):c.797T>C (p.Phe266Ser)	rs141587158	0.00273
NM_000341.4(SLC3A1):c.231T>A (p.Ser77=)	rs146630359	0.00250
NM_000341.4(SLC3A1):c.1398C>T (p.Asn466=)	rs140821819	0.00211
NM_000341.4(SLC3A1):c.1333-12T>A	rs183158004	0.00150
NM_000341.4(SLC3A1):c.672A>G (p.Gln224=)	rs140331858	0.00111
NM_000341.4(SLC3A1):c.1381T>C (p.Tyr461His)	rs144162964	0.00044
NM_000341.4(SLC3A1):c.66C>T (p.Asn22=)	rs149507807	0.00026
NM_000341.4(SLC3A1):c.765+15G>A	rs541948214	0.00020
NM_000341.4(SLC3A1):c.1149T>C (p.Thr383=)	rs369948288	0.00008
NM_000341.4(SLC3A1):c.1136+3del	rs796262035
NM_000341.4(SLC3A1):c.892-17T>G
NM_000341.4(SLC3A1):c.892-17del	rs551929018

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