ClinVar Miner

List of variants in gene CLCN1 reported as likely benign for not specified

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Total variants: 32
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HGVS dbSNP
NM_000083.3(CLCN1):c.1065-16T>C rs113764654
NM_000083.3(CLCN1):c.1392C>T (p.Phe464=) rs201919331
NM_000083.3(CLCN1):c.13C>T (p.Arg5Trp) rs1322496244
NM_000083.3(CLCN1):c.1482T>C (p.Phe494=) rs745690349
NM_000083.3(CLCN1):c.153C>T (p.Gly51=) rs1554433799
NM_000083.3(CLCN1):c.1583-12G>A rs374736253
NM_000083.3(CLCN1):c.1593G>A (p.Ala531=) rs367696668
NM_000083.3(CLCN1):c.1605C>T (p.Ala535=) rs200676193
NM_000083.3(CLCN1):c.1815T>C (p.Val605=) rs141945240
NM_000083.3(CLCN1):c.1863A>G (p.Thr621=) rs369099862
NM_000083.3(CLCN1):c.1977C>A (p.Ala659=) rs904572417
NM_000083.3(CLCN1):c.2230C>A (p.Pro744Thr) rs149316679
NM_000083.3(CLCN1):c.2284+19G>A rs769666294
NM_000083.3(CLCN1):c.2284+5C>T rs74824159
NM_000083.3(CLCN1):c.2364+10G>A rs201855153
NM_000083.3(CLCN1):c.2509-16T>G rs774042985
NM_000083.3(CLCN1):c.2509-3C>T rs375341574
NM_000083.3(CLCN1):c.2541C>T (p.His847=) rs146653916
NM_000083.3(CLCN1):c.2847C>T (p.Gly949=) rs760793323
NM_000083.3(CLCN1):c.2883G>C (p.Gly961=) rs1057522756
NM_000083.3(CLCN1):c.2937C>T (p.Asp979=) rs776873546
NM_000083.3(CLCN1):c.316C>G (p.Leu106Val) rs145517198
NM_000083.3(CLCN1):c.434-14A>G rs200263856
NM_000083.3(CLCN1):c.501C>G (p.Phe167Leu) rs149729531
NM_000083.3(CLCN1):c.633C>T (p.Ala211=) rs138246784
NM_000083.3(CLCN1):c.651C>T (p.Val217=) rs144109732
NM_000083.3(CLCN1):c.655C>T (p.Leu219=) rs1427322271
NM_000083.3(CLCN1):c.720C>T (p.Ser240=) rs764402957
NM_000083.3(CLCN1):c.804G>A (p.Thr268=) rs141521078
NM_000083.3(CLCN1):c.854-8C>T rs201115855
NM_000083.3(CLCN1):c.86A>C (p.His29Pro) rs146160029
NM_000083.3(CLCN1):c.900G>A (p.Arg300=) rs149578972

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