ClinVar Miner

List of variants in gene LINS1 reported as likely benign by Ambry Genetics

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Gene type:
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Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_001040616.3(LINS1):c.2034A>G (p.Pro678=) rs1047320 0.01811
NM_001040616.3(LINS1):c.1285C>T (p.Leu429=) rs141962847 0.00463
NM_001040616.3(LINS1):c.718C>T (p.Arg240Trp) rs145145735 0.00398
NM_001040616.3(LINS1):c.1887C>T (p.Tyr629=) rs61999313 0.00313
NM_001040616.3(LINS1):c.1302G>A (p.Pro434=) rs148166631 0.00269
NM_001040616.3(LINS1):c.1813A>G (p.Met605Val) rs141855950 0.00249
NM_001040616.3(LINS1):c.1194A>G (p.Gln398=) rs138347314 0.00244
NM_001040616.3(LINS1):c.2119G>A (p.Gly707Arg) rs74039425 0.00213
NM_001040616.3(LINS1):c.1124C>T (p.Thr375Ile) rs143097819 0.00187
NM_001040616.3(LINS1):c.615A>G (p.Ser205=) rs148622636 0.00081
NM_001040616.3(LINS1):c.267G>A (p.Met89Ile) rs150280970 0.00071
NM_001040616.3(LINS1):c.1851G>T (p.Leu617=) rs146405261 0.00054
NM_001040616.3(LINS1):c.864C>T (p.Thr288=) rs150775570 0.00051
NM_001040616.3(LINS1):c.1479T>C (p.Cys493=) rs144513217 0.00036
NM_001040616.3(LINS1):c.312G>A (p.Leu104=) rs61741890 0.00030
NM_001040616.3(LINS1):c.987T>C (p.His329=) rs192389870 0.00016
NM_001040616.3(LINS1):c.2107G>A (p.Val703Ile) rs567942281 0.00011
NM_001040616.3(LINS1):c.993G>A (p.Ala331=) rs767030288 0.00006
NM_001040616.3(LINS1):c.807T>C (p.His269=) rs747513969 0.00002
NM_001040616.3(LINS1):c.1296C>T (p.His432=)
NM_001040616.3(LINS1):c.1320G>A (p.Arg440=) rs1567713840
NM_001040616.3(LINS1):c.1668T>C (p.Ile556=)
NM_001040616.3(LINS1):c.205A>G (p.Ile69Val)
NM_001040616.3(LINS1):c.2121A>T (p.Gly707=)
NM_001040616.3(LINS1):c.2163T>C (p.Asp721=)
NM_001040616.3(LINS1):c.2178G>A (p.Leu726=)
NM_001040616.3(LINS1):c.228G>A (p.Leu76=)
NM_001040616.3(LINS1):c.651G>C (p.Leu217=)
NM_001040616.3(LINS1):c.975G>A (p.Pro325=)

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