ClinVar Miner

List of variants in gene LINS1 reported as uncertain significance by Ambry Genetics

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Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_001040616.3(LINS1):c.52G>A (p.Gly18Arg) rs141782332 0.00215
NM_001040616.3(LINS1):c.2027A>G (p.Glu676Gly) rs150348863 0.00101
NM_001040616.3(LINS1):c.1940G>A (p.Ser647Asn) rs150317593 0.00073
NM_001040616.3(LINS1):c.1888G>A (p.Asp630Asn) rs61999316 0.00041
NM_001040616.3(LINS1):c.1993G>A (p.Gly665Arg) rs140140023 0.00037
NM_001040616.3(LINS1):c.554A>G (p.Asn185Ser) rs146704559 0.00018
NM_001040616.3(LINS1):c.1013C>T (p.Ala338Val) rs763210104 0.00014
NM_001040616.3(LINS1):c.418T>A (p.Ser140Thr) rs200152794 0.00009
NM_001040616.3(LINS1):c.1481T>C (p.Ile494Thr) rs772460402 0.00006
NM_001040616.3(LINS1):c.1347G>A (p.Met449Ile) rs201677311 0.00005
NM_001040616.3(LINS1):c.1981C>G (p.Gln661Glu) rs779605614 0.00003
NM_001040616.3(LINS1):c.842C>G (p.Ser281Cys) rs779725468 0.00003
NM_001040616.3(LINS1):c.1121T>C (p.Ile374Thr) rs776962968 0.00001
NM_001040616.3(LINS1):c.1169T>C (p.Met390Thr) rs765705767 0.00001
NM_001040616.3(LINS1):c.1222G>A (p.Val408Ile) rs1273162899 0.00001
NM_001040616.3(LINS1):c.661G>A (p.Asp221Asn) rs1567718073 0.00001
NM_001040616.3(LINS1):c.-5T>A
NM_001040616.3(LINS1):c.1007C>G (p.Ala336Gly)
NM_001040616.3(LINS1):c.1007C>T (p.Ala336Val)
NM_001040616.3(LINS1):c.1064T>G (p.Val355Gly)
NM_001040616.3(LINS1):c.1133A>G (p.Asp378Gly)
NM_001040616.3(LINS1):c.1173A>C (p.Lys391Asn)
NM_001040616.3(LINS1):c.1298A>G (p.Asn433Ser) rs756749166
NM_001040616.3(LINS1):c.1301C>T (p.Pro434Leu)
NM_001040616.3(LINS1):c.1353G>C (p.Glu451Asp)
NM_001040616.3(LINS1):c.1394+4A>G rs200846434
NM_001040616.3(LINS1):c.1491CTT[1] (p.Phe498del)
NM_001040616.3(LINS1):c.1505T>C (p.Ile502Thr)
NM_001040616.3(LINS1):c.1534T>A (p.Phe512Ile)
NM_001040616.3(LINS1):c.1568A>G (p.Tyr523Cys)
NM_001040616.3(LINS1):c.1660A>G (p.Ile554Val)
NM_001040616.3(LINS1):c.172A>G (p.Arg58Gly)
NM_001040616.3(LINS1):c.194G>A (p.Gly65Asp)
NM_001040616.3(LINS1):c.2008A>G (p.Lys670Glu)
NM_001040616.3(LINS1):c.2080G>T (p.Asp694Tyr)
NM_001040616.3(LINS1):c.2173C>T (p.Arg725Cys)
NM_001040616.3(LINS1):c.2183A>G (p.Lys728Arg)
NM_001040616.3(LINS1):c.2270T>A (p.Leu757Ter) rs1383641417
NM_001040616.3(LINS1):c.271C>T (p.Leu91Phe)
NM_001040616.3(LINS1):c.392C>G (p.Ser131Cys)
NM_001040616.3(LINS1):c.399+4A>G
NM_001040616.3(LINS1):c.525G>T (p.Gln175His)
NM_001040616.3(LINS1):c.550A>C (p.Ser184Arg)
NM_001040616.3(LINS1):c.607A>G (p.Lys203Glu)
NM_001040616.3(LINS1):c.632A>G (p.Glu211Gly)
NM_001040616.3(LINS1):c.778A>G (p.Ile260Val) rs1291611710
NM_001040616.3(LINS1):c.781G>A (p.Ala261Thr)
NM_001040616.3(LINS1):c.917G>T (p.Cys306Phe)

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