ClinVar Miner

List of variants in gene CWC27 reported as benign for not provided

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Gene type:
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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_005869.4(CWC27):c.139+3_139+4insAATTATGAC rs140062546 0.52488
NM_005869.4(CWC27):c.766C>G (p.Pro256Ala) rs7735338 0.36437
NM_005869.4(CWC27):c.749+16G>T rs6449760 0.35252
NM_005869.4(CWC27):c.1108T>C (p.Leu370=) rs2278351 0.27219
NM_005869.4(CWC27):c.1042+7G>A rs73105301 0.01166
NM_005869.4(CWC27):c.670-20A>C rs10062054 0.00951
NM_005869.4(CWC27):c.670-6T>C rs10055003 0.00951
NM_005869.4(CWC27):c.1074C>G (p.Ala358=) rs58322956 0.00892
NM_005869.4(CWC27):c.1042+18G>A rs114182066 0.00511
NM_005869.4(CWC27):c.1153-17T>C rs181922845 0.00130
NM_005869.4(CWC27):c.1042+17C>T rs201575731 0.00121
NM_005869.4(CWC27):c.750-18T>G rs201763486 0.00114
NM_005869.4(CWC27):c.496-14del rs543492497 0.00047
NM_005869.4(CWC27):c.253-18A>C rs759616532 0.00024
NM_005869.4(CWC27):c.1209G>A (p.Thr403=) rs1309581
NM_005869.4(CWC27):c.1209G>T (p.Thr403=) rs1309581
NM_005869.4(CWC27):c.140-4del rs200915173
NM_005869.4(CWC27):c.140-4dup rs200915173
NM_005869.4(CWC27):c.600-8del
NM_005869.4(CWC27):c.669+18_669+25del rs369020972
NM_005869.4(CWC27):c.750-3T>C rs191441227
NM_005869.4(CWC27):c.750-5dup rs771898756
NM_005869.4(CWC27):c.781-13dup rs760410222
NM_005869.4(CWC27):c.938+3212_938+3213dup
NM_005869.4(CWC27):c.939-10del

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