List of variants in gene combination PREPL, SLC3A1 reported as uncertain significance for not provided

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000341.4(SLC3A1):c.1846G>A (p.Ala616Thr)	rs143740561	0.00050
NM_001171613.2(PREPL):c.1844A>G (p.Lys615Arg)	rs138348037	0.00049
NM_000341.4(SLC3A1):c.1973G>A (p.Arg658His)	rs370262167	0.00011
NM_000341.4(SLC3A1):c.1843C>A (p.Pro615Thr)	rs121912696	0.00001
NM_000341.4(SLC3A1):c.1735T>G (p.Tyr579Asp)
NM_000341.4(SLC3A1):c.2027G>A (p.Ser676Asn)	rs750128585
NM_001171613.2(PREPL):c.1827+5G>A	rs1672986669
NM_001171613.2(PREPL):c.1848C>G (p.Phe616Leu)
NM_001171613.2(PREPL):c.1850T>C (p.Leu617Pro)	rs537620020

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