ClinVar Miner

List of variants in gene LAMA4 reported as uncertain significance by Biesecker Lab/Human Development Section,National Institutes of Health

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Total variants: 21
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HGVS dbSNP
NM_001105206.2(LAMA4):c.2614C>G (p.Pro872Ala) rs180931319
NM_002290.4(LAMA4):c.1066G>C (p.Ala356Pro) rs201431982
NM_002290.4(LAMA4):c.1454T>A (p.Leu485His) rs3752579
NM_002290.4(LAMA4):c.1837G>A (p.Ala613Thr) rs374001056
NM_002290.4(LAMA4):c.2156A>T (p.Asp719Val) rs781823199
NM_002290.4(LAMA4):c.2891C>T (p.Ser964Phe) rs781856644
NM_002290.4(LAMA4):c.3005C>A (p.Ala1002Asp) rs199618820
NM_002290.4(LAMA4):c.3008C>T (p.Thr1003Ile) rs201431614
NM_002290.4(LAMA4):c.3053A>G (p.Tyr1018Cys) rs370557242
NM_002290.4(LAMA4):c.3154G>A (p.Val1052Met) rs373650093
NM_002290.4(LAMA4):c.3301C>T (p.His1101Tyr) rs201660110
NM_002290.4(LAMA4):c.3564T>A (p.Asp1188Glu) rs786205410
NM_002290.4(LAMA4):c.3922G>A (p.Val1308Ile) rs70940811
NM_002290.4(LAMA4):c.4147C>T (p.Arg1383Trp) rs200189282
NM_002290.4(LAMA4):c.4307C>T (p.Ala1436Val) rs782696599
NM_002290.4(LAMA4):c.4687G>T (p.Asp1563Tyr) rs199938033
NM_002290.4(LAMA4):c.521A>G (p.Tyr174Cys) rs202131320
NM_002290.4(LAMA4):c.5348C>T (p.Thr1783Ile) rs786205409
NM_002290.4(LAMA4):c.5416G>A (p.Gly1806Ser) rs142048329
NM_002290.4(LAMA4):c.676C>T (p.Pro226Ser) rs201820268
NM_002290.4(LAMA4):c.811T>C (p.Trp271Arg) rs201486893

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