ClinVar Miner

List of variants in gene LAS1L reported as uncertain significance for developmental disorder of mental health

Included ClinVar conditions (728):
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Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_031206.7(LAS1L):c.1735G>A (p.Val579Ile) rs200862250 0.00019
NM_031206.7(LAS1L):c.1705A>G (p.Lys569Glu) rs1006077682 0.00010
NM_031206.7(LAS1L):c.754G>A (p.Val252Met) rs762043715 0.00007
NM_031206.7(LAS1L):c.940G>A (p.Val314Ile) rs137948118 0.00007
NM_031206.7(LAS1L):c.1892G>C (p.Gly631Ala) rs371394378 0.00005
NM_031206.7(LAS1L):c.937G>A (p.Gly313Ser) rs745313876 0.00005
NM_031206.7(LAS1L):c.1270G>A (p.Val424Ile) rs761006702 0.00002
NM_031206.7(LAS1L):c.1282G>A (p.Val428Met) rs1190754458 0.00002
NM_031206.7(LAS1L):c.1483G>A (p.Glu495Lys) rs762931496 0.00002
NM_031206.7(LAS1L):c.715G>T (p.Asp239Tyr) rs750436732 0.00002
NM_031206.7(LAS1L):c.1871G>A (p.Arg624Lys) rs370120927 0.00001
NM_031206.7(LAS1L):c.674A>G (p.Gln225Arg) rs758854025 0.00001
NM_031206.7(LAS1L):c.948C>T (p.Cys316=) rs1410871672 0.00001
NM_031206.7(LAS1L):c.1082C>G (p.Pro361Arg) rs867562406
NM_031206.7(LAS1L):c.1083A>G (p.Pro361=)
NM_031206.7(LAS1L):c.1114G>C (p.Val372Leu) rs186130633
NM_031206.7(LAS1L):c.1129C>G (p.Pro377Ala)
NM_031206.7(LAS1L):c.1203G>T (p.Arg401Ser) rs1569438242
NM_031206.7(LAS1L):c.1285G>A (p.Ala429Thr)
NM_031206.7(LAS1L):c.1298C>T (p.Thr433Ile) rs2068997748
NM_031206.7(LAS1L):c.1301-10T>C
NM_031206.7(LAS1L):c.1472G>A (p.Gly491Asp) rs1556301877
NM_031206.7(LAS1L):c.1505G>A (p.Arg502His)
NM_031206.7(LAS1L):c.1570C>A (p.Pro524Thr)
NM_031206.7(LAS1L):c.1570C>G (p.Pro524Ala) rs2068725707
NM_031206.7(LAS1L):c.1571C>A (p.Pro524His)
NM_031206.7(LAS1L):c.1613G>A (p.Ser538Asn)
NM_031206.7(LAS1L):c.1764AGAGGAGGA[1] (p.Glu591_Glu593del) rs747219544
NM_031206.7(LAS1L):c.1822G>T (p.Val608Leu)
NM_031206.7(LAS1L):c.1837A>G (p.Thr613Ala) rs2148270110
NM_031206.7(LAS1L):c.1889G>T (p.Arg630Ile) rs2148270017
NM_031206.7(LAS1L):c.1961G>T (p.Arg654Leu) rs1556298998
NM_031206.7(LAS1L):c.2050C>T (p.Arg684Trp) rs762602796
NM_031206.7(LAS1L):c.2051G>A (p.Arg684Gln) rs900809839
NM_031206.7(LAS1L):c.2057A>G (p.Glu686Gly)
NM_031206.7(LAS1L):c.2104G>A (p.Gly702Ser)
NM_031206.7(LAS1L):c.2176G>A (p.Gly726Arg)
NM_031206.7(LAS1L):c.311G>T (p.Gly104Val)
NM_031206.7(LAS1L):c.320G>A (p.Gly107Asp) rs2069620231
NM_031206.7(LAS1L):c.43G>C (p.Gly15Arg)
NM_031206.7(LAS1L):c.502G>A (p.Asp168Asn) rs1569443405
NM_031206.7(LAS1L):c.515-6C>G rs1379421207
NM_031206.7(LAS1L):c.663C>A (p.Asp221Glu) rs778389447
NM_031206.7(LAS1L):c.704G>A (p.Ser235Asn) rs755168381
NM_031206.7(LAS1L):c.706A>G (p.Thr236Ala) rs2069367677
NM_031206.7(LAS1L):c.727G>A (p.Asp243Asn)
NM_031206.7(LAS1L):c.942_956+6dup
NM_031206.7(LAS1L):c.947G>A (p.Cys316Tyr)
NM_031206.7(LAS1L):c.949G>A (p.Glu317Lys)

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