ClinVar Miner

List of variants in gene CLCC1 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 117
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HGVS dbSNP gnomAD frequency
NM_001377458.1(CLCC1):c.478A>C (p.Ile160Leu) rs141270237 0.00160
NM_001377458.1(CLCC1):c.1486C>G (p.Pro496Ala) rs151247614 0.00112
NM_001377458.1(CLCC1):c.643C>T (p.Arg215Cys) rs144374978 0.00083
NM_001377458.1(CLCC1):c.1480G>A (p.Ala494Thr) rs144141792 0.00053
NM_001377458.1(CLCC1):c.1542G>A (p.Lys514=) rs150029224 0.00050
NM_001377458.1(CLCC1):c.855C>G (p.Leu285=) rs145581622 0.00047
NM_001377458.1(CLCC1):c.797-8C>T rs369689028 0.00036
NM_001377458.1(CLCC1):c.934T>C (p.Leu312=) rs142773865 0.00026
NM_001377458.1(CLCC1):c.1530C>T (p.Pro510=) rs751379265 0.00015
NM_001377458.1(CLCC1):c.1347C>T (p.Asp449=) rs576849616 0.00014
NM_001377458.1(CLCC1):c.797-16C>A rs184874100 0.00012
NM_001377458.1(CLCC1):c.1556C>G (p.Ser519Cys) rs147516957 0.00011
NM_001377458.1(CLCC1):c.895-18G>C rs372170284 0.00011
NM_001377458.1(CLCC1):c.1488T>C (p.Pro496=) rs201091112 0.00010
NM_001377458.1(CLCC1):c.522C>T (p.Phe174=) rs138361021 0.00007
NM_001377458.1(CLCC1):c.1155T>C (p.Ile385=) rs200641997 0.00006
NM_001377458.1(CLCC1):c.1432C>T (p.Leu478=) rs377215045 0.00006
NM_001377458.1(CLCC1):c.1449G>A (p.Pro483=) rs776756029 0.00005
NM_001377458.1(CLCC1):c.129+16C>T rs201078487 0.00004
NM_001377458.1(CLCC1):c.129+17G>A rs377328396 0.00004
NM_001377458.1(CLCC1):c.1384-5T>C rs375961109 0.00004
NM_001377458.1(CLCC1):c.895-8C>T rs755934535 0.00004
NM_001377458.1(CLCC1):c.1362G>A (p.Glu454=) rs760884698 0.00003
NM_001377458.1(CLCC1):c.895-7G>A rs750268664 0.00003
NM_001377458.1(CLCC1):c.909A>C (p.Thr303=) rs571666014 0.00003
NM_001377458.1(CLCC1):c.1080G>A (p.Leu360=) rs1047015131 0.00002
NM_001377458.1(CLCC1):c.1599C>T (p.Pro533=) rs778079497 0.00002
NM_001377458.1(CLCC1):c.204T>C (p.Tyr68=) rs761645768 0.00002
NM_001377458.1(CLCC1):c.231+9T>C rs772563788 0.00002
NM_001377458.1(CLCC1):c.664C>T (p.Leu222=) rs1198329648 0.00002
NM_001377458.1(CLCC1):c.903A>G (p.Ala301=) rs757150346 0.00002
NM_001377458.1(CLCC1):c.1188C>T (p.Ala396=) rs757643802 0.00001
NM_001377458.1(CLCC1):c.1200T>C (p.Tyr400=) rs562334230 0.00001
NM_001377458.1(CLCC1):c.130-16C>G rs1425738401 0.00001
NM_001377458.1(CLCC1):c.1479G>A (p.Ser493=) rs1238945398 0.00001
NM_001377458.1(CLCC1):c.198A>G (p.Glu66=) rs752747251 0.00001
NM_001377458.1(CLCC1):c.231+14T>A rs748602461 0.00001
NM_001377458.1(CLCC1):c.37C>T (p.Leu13=) rs780313648 0.00001
NM_001377458.1(CLCC1):c.423C>T (p.Leu141=) rs905396583 0.00001
NM_001377458.1(CLCC1):c.585C>T (p.Ile195=) rs1169805673 0.00001
NM_001377458.1(CLCC1):c.618T>C (p.Tyr206=) rs769540698 0.00001
NM_001377458.1(CLCC1):c.702+19G>T rs755357047 0.00001
NM_001377458.1(CLCC1):c.819C>G (p.Thr273=) rs1456673755 0.00001
NM_001377458.1(CLCC1):c.852G>A (p.Glu284=) rs1224265138 0.00001
NM_001377458.1(CLCC1):c.942T>C (p.His314=) rs1297754654 0.00001
NM_001377458.1(CLCC1):c.1030T>C (p.Leu344=)
NM_001377458.1(CLCC1):c.1041+7A>G rs2101637473
NM_001377458.1(CLCC1):c.1042-20T>C
NM_001377458.1(CLCC1):c.1059T>G (p.Ala353=) rs2101626892
NM_001377458.1(CLCC1):c.1074T>C (p.His358=)
NM_001377458.1(CLCC1):c.1134T>C (p.Asp378=)
NM_001377458.1(CLCC1):c.1167T>C (p.Pro389=) rs1653158784
NM_001377458.1(CLCC1):c.1215C>G (p.Gly405=)
NM_001377458.1(CLCC1):c.1215C>T (p.Gly405=)
NM_001377458.1(CLCC1):c.1230C>T (p.Gly410=) rs2101626075
NM_001377458.1(CLCC1):c.1245G>A (p.Thr415=)
NM_001377458.1(CLCC1):c.1267T>C (p.Leu423=)
NM_001377458.1(CLCC1):c.130-14A>T
NM_001377458.1(CLCC1):c.130-9_130-8del rs1654983611
NM_001377458.1(CLCC1):c.1338T>C (p.Asp446=) rs898425062
NM_001377458.1(CLCC1):c.1377A>G (p.Val459=) rs2101625394
NM_001377458.1(CLCC1):c.1383+14T>A
NM_001377458.1(CLCC1):c.1384-12T>C
NM_001377458.1(CLCC1):c.1384-17A>G
NM_001377458.1(CLCC1):c.1384-19G>A
NM_001377458.1(CLCC1):c.1384-8_1384-4dup
NM_001377458.1(CLCC1):c.138T>C (p.Tyr46=) rs1311026750
NM_001377458.1(CLCC1):c.1464T>G (p.Thr488=) rs1652645485
NM_001377458.1(CLCC1):c.1482C>T (p.Ala494=) rs372290951
NM_001377458.1(CLCC1):c.1518A>G (p.Thr506=)
NM_001377458.1(CLCC1):c.1536G>A (p.Ala512=)
NM_001377458.1(CLCC1):c.1563C>A (p.Ala521=) rs775931647
NM_001377458.1(CLCC1):c.1563C>T (p.Ala521=)
NM_001377458.1(CLCC1):c.1596C>T (p.Ser532=) rs1185224785
NM_001377458.1(CLCC1):c.1620A>T (p.Pro540=)
NM_001377458.1(CLCC1):c.1635G>A (p.Pro545=) rs145636232
NM_001377458.1(CLCC1):c.1635G>C (p.Pro545=) rs145636232
NM_001377458.1(CLCC1):c.1635G>T (p.Pro545=) rs145636232
NM_001377458.1(CLCC1):c.228T>C (p.Tyr76=)
NM_001377458.1(CLCC1):c.231+19A>G rs2101682208
NM_001377458.1(CLCC1):c.232-10A>G rs760324712
NM_001377458.1(CLCC1):c.232-7G>A
NM_001377458.1(CLCC1):c.232-7G>T
NM_001377458.1(CLCC1):c.306T>C (p.Asn102=)
NM_001377458.1(CLCC1):c.339+11G>C rs2101673022
NM_001377458.1(CLCC1):c.340-23_340-20del rs779270419
NM_001377458.1(CLCC1):c.340-6_340-2del rs546311673
NM_001377458.1(CLCC1):c.399T>C (p.Thr133=) rs2101656107
NM_001377458.1(CLCC1):c.435C>T (p.Asp145=)
NM_001377458.1(CLCC1):c.456T>C (p.Asp152=)
NM_001377458.1(CLCC1):c.45T>C (p.Ala15=)
NM_001377458.1(CLCC1):c.463C>T (p.Leu155=)
NM_001377458.1(CLCC1):c.465A>G (p.Leu155=)
NM_001377458.1(CLCC1):c.513G>A (p.Lys171=)
NM_001377458.1(CLCC1):c.528T>C (p.Asp176=)
NM_001377458.1(CLCC1):c.534T>C (p.Phe178=)
NM_001377458.1(CLCC1):c.561+18C>T rs749125967
NM_001377458.1(CLCC1):c.562-17C>T rs2101654230
NM_001377458.1(CLCC1):c.562-6T>C
NM_001377458.1(CLCC1):c.621A>T (p.Val207=) rs1422141232
NM_001377458.1(CLCC1):c.630C>T (p.Tyr210=) rs2101653754
NM_001377458.1(CLCC1):c.702+8A>G
NM_001377458.1(CLCC1):c.703-19C>G
NM_001377458.1(CLCC1):c.792C>T (p.Ile264=)
NM_001377458.1(CLCC1):c.797-10C>T
NM_001377458.1(CLCC1):c.797-13T>C
NM_001377458.1(CLCC1):c.797-6A>C rs1374973815
NM_001377458.1(CLCC1):c.797-6A>G
NM_001377458.1(CLCC1):c.846C>T (p.Tyr282=) rs1653647113
NM_001377458.1(CLCC1):c.849T>C (p.Tyr283=) rs1317288089
NM_001377458.1(CLCC1):c.882C>A (p.Val294=)
NM_001377458.1(CLCC1):c.882C>T (p.Val294=)
NM_001377458.1(CLCC1):c.894+18T>C
NM_001377458.1(CLCC1):c.897A>G (p.Ala299=) rs2101638131
NM_001377458.1(CLCC1):c.924A>C (p.Val308=)
NM_001377458.1(CLCC1):c.927G>A (p.Thr309=) rs146056637
NM_001377458.1(CLCC1):c.966T>C (p.Phe322=) rs2101637804

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