List of variants in gene SLC1A3 reported as uncertain significance for not specified

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_004172.5(SLC1A3):c.1496G>A (p.Arg499Gln)	rs138085358	0.00007
NM_004172.5(SLC1A3):c.1177G>A (p.Val393Ile)	rs549250283	0.00003
NM_004172.5(SLC1A3):c.685G>A (p.Glu229Lys)	rs974656218	0.00002
NM_004172.5(SLC1A3):c.1285A>G (p.Ile429Val)	rs1391192851	0.00001
NM_004172.5(SLC1A3):c.1450G>A (p.Val484Ile)	rs549164007	0.00001
NM_004172.5(SLC1A3):c.1612A>T (p.Ser538Cys)	rs752803485	0.00001
NM_004172.5(SLC1A3):c.319+3A>G	rs747858400	0.00001
NM_004172.5(SLC1A3):c.1290-15T>C	rs2478179875
NM_004172.5(SLC1A3):c.590G>A (p.Arg197Lys)	rs1554045196
NM_004172.5(SLC1A3):c.664G>T (p.Glu222Ter)	rs1382977672

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