ClinVar Miner

List of variants in gene LAMA4 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_001105206.3(LAMA4):c.422+20G>T rs188820838 0.00271
NM_001105206.3(LAMA4):c.4314A>C (p.Ser1438=) rs77367833 0.00251
NM_001105206.3(LAMA4):c.5016T>A (p.Ile1672=) rs148517180 0.00210
NM_001105206.3(LAMA4):c.2493+15G>T rs77901141 0.00178
NM_001105206.3(LAMA4):c.196-9C>T rs144850734 0.00174
NM_001105206.3(LAMA4):c.4822-3C>T rs191447048 0.00151
NM_001105206.3(LAMA4):c.514G>A (p.Gly172Ser) rs147695488 0.00091
NM_001105206.3(LAMA4):c.674C>T (p.Ala225Val) rs149615862 0.00052
NM_001105206.3(LAMA4):c.5340A>G (p.Thr1780=) rs139241892 0.00050
NM_001105206.3(LAMA4):c.196-11G>A rs374364713 0.00007
NM_001105206.3(LAMA4):c.1551+8G>A rs782128294 0.00006
NM_001105206.3(LAMA4):c.672C>T (p.Cys224=) rs781903380 0.00006
NM_001105206.3(LAMA4):c.5029C>T (p.Arg1677Cys) rs587753056 0.00002
NM_001105206.3(LAMA4):c.267C>T (p.Asn89=) rs727503114 0.00001
NM_001105206.3(LAMA4):c.4977T>C (p.Val1659=) rs199593652 0.00001
NM_001105206.3(LAMA4):c.1419C>T (p.Val473=) rs782796474
NM_001105206.3(LAMA4):c.373G>T (p.Ala125Ser) rs529185662
NM_001105206.3(LAMA4):c.730G>C (p.Gly244Arg) rs147078770
NM_001105206.3(LAMA4):c.85G>C (p.Asp29His) rs150662822

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