ClinVar Miner

List of variants in gene LAMA5 reported as uncertain significance by GeneDx

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_005560.6(LAMA5):c.6940C>T (p.Arg2314Trp) rs201303962 0.00031
NM_005560.6(LAMA5):c.7637C>T (p.Ala2546Val) rs147692310 0.00017
NM_005560.6(LAMA5):c.1717C>T (p.Arg573Cys) rs200807853 0.00007
NM_005560.6(LAMA5):c.4879C>T (p.Arg1627Cys) rs139955074 0.00007
NM_005560.6(LAMA5):c.371C>T (p.Thr124Met) rs781700836 0.00006
NM_005560.6(LAMA5):c.4978C>T (p.Arg1660Trp) rs770477724 0.00006
NM_005560.6(LAMA5):c.2240G>A (p.Arg747Gln) rs201992387 0.00005
NM_005560.6(LAMA5):c.2659C>T (p.His887Tyr) rs777193671 0.00005
NM_005560.6(LAMA5):c.7132G>A (p.Glu2378Lys) rs763121557 0.00005
NM_005560.6(LAMA5):c.9058C>G (p.Leu3020Val) rs138425104 0.00005
NM_005560.6(LAMA5):c.3502G>T (p.Asp1168Tyr) rs138669003 0.00003
NM_005560.6(LAMA5):c.6383C>T (p.Thr2128Met) rs368757053 0.00003
NM_005560.6(LAMA5):c.7121T>C (p.Leu2374Pro) rs1368343307 0.00002
NM_005560.6(LAMA5):c.1282+3G>T rs778162852
NM_005560.6(LAMA5):c.1502C>T (p.Thr501Ile)
NM_005560.6(LAMA5):c.2606C>T (p.Pro869Leu)
NM_005560.6(LAMA5):c.404G>A (p.Arg135His)
NM_005560.6(LAMA5):c.4409G>A (p.Arg1470His)
NM_005560.6(LAMA5):c.4627T>C (p.Cys1543Arg) rs2516066874
NM_005560.6(LAMA5):c.5460C>T (p.Gly1820=) rs1555876117
NM_005560.6(LAMA5):c.5575G>A (p.Gly1859Ser)
NM_005560.6(LAMA5):c.6659G>T (p.Arg2220Leu) rs150944918
NM_005560.6(LAMA5):c.7154G>A (p.Arg2385Gln) rs145597795
NM_005560.6(LAMA5):c.7613C>T (p.Ala2538Val)
NM_005560.6(LAMA5):c.9078G>A (p.Ala3026=)
NM_005560.6(LAMA5):c.928G>A (p.Asp310Asn) rs370325282

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