ClinVar Miner

List of variants in gene LAMP2 reported as uncertain significance for not provided

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Total variants: 22
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HGVS dbSNP
NM_002294.2(LAMP2):c.1000G>C (p.Glu334Gln) rs766962315
NM_002294.2(LAMP2):c.1040C>G (p.Thr347Ser) rs730880487
NM_002294.2(LAMP2):c.1114_1116GAC[1] (p.Asp373del) rs730880494
NM_002294.2(LAMP2):c.23C>G (p.Pro8Arg) rs878854484
NM_002294.2(LAMP2):c.23C>T (p.Pro8Leu) rs878854484
NM_002294.2(LAMP2):c.260A>C (p.Lys87Thr) rs1556112678
NM_002294.2(LAMP2):c.320C>G (p.Ser107Cys) rs730880497
NM_002294.2(LAMP2):c.339C>G (p.Ser113Arg) rs147369153
NM_002294.2(LAMP2):c.364G>A (p.Asp122Asn) rs730880480
NM_002294.2(LAMP2):c.385G>A (p.Ala129Thr) rs149276836
NM_002294.2(LAMP2):c.461A>G (p.Asn154Ser) rs773525538
NM_002294.2(LAMP2):c.472A>G (p.Thr158Ala) rs138374063
NM_002294.2(LAMP2):c.515T>C (p.Leu172Pro) rs371174243
NM_002294.2(LAMP2):c.556+13T>A
NM_002294.2(LAMP2):c.586A>T (p.Thr196Ser) rs138991195
NM_002294.2(LAMP2):c.715C>G (p.Leu239Val) rs730880481
NM_002294.2(LAMP2):c.73C>T (p.Arg25Trp) rs730880478
NM_002294.2(LAMP2):c.769A>G (p.Asn257Asp) rs369032377
NM_002294.2(LAMP2):c.797G>A (p.Arg266His) rs200934351
NM_002294.2(LAMP2):c.805A>G (p.Thr269Ala) rs1131691290
NM_002294.2(LAMP2):c.887T>C (p.Leu296Pro) rs730880486
NM_002294.2(LAMP2):c.8G>A (p.Cys3Tyr) rs730880489

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