ClinVar Miner

List of variants in gene CDH23 reported as likely benign for not provided

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Total variants: 23
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HGVS dbSNP
NM_022124.6(CDH23):c.10044C>G (p.Pro3348=) rs370568585
NM_022124.6(CDH23):c.1096G>A (p.Ala366Thr) rs143282422
NM_022124.6(CDH23):c.1135-7T>C rs397517303
NM_022124.6(CDH23):c.1263C>T (p.Tyr421=)
NM_022124.6(CDH23):c.1291-89C>T
NM_022124.6(CDH23):c.1753-7C>T
NM_022124.6(CDH23):c.2289+3G>A
NM_022124.6(CDH23):c.3074G>A (p.Gly1025Asp) rs143179070
NM_022124.6(CDH23):c.4287C>T (p.Pro1429=) rs377493327
NM_022124.6(CDH23):c.5026G>A (p.Ala1676Thr) rs56043301
NM_022124.6(CDH23):c.5418C>G (p.Asp1806Glu) rs74145660
NM_022124.6(CDH23):c.5544C>T (p.Asp1848=) rs142131750
NM_022124.6(CDH23):c.5604C>T (p.Ser1868=)
NM_022124.6(CDH23):c.5924-90G>A
NM_022124.6(CDH23):c.6329C>T (p.Ala2110Val) rs111033492
NM_022124.6(CDH23):c.6596T>A (p.Ile2199Asn) rs111033494
NM_022124.6(CDH23):c.6990G>T (p.Leu2330=) rs111033495
NM_022124.6(CDH23):c.7630T>C (p.Leu2544=) rs114819374
NM_022124.6(CDH23):c.8283C>T (p.Asn2761=)
NM_022124.6(CDH23):c.8444G>A (p.Arg2815His)
NM_022124.6(CDH23):c.8980-12C>T rs111583276
NM_022124.6(CDH23):c.9077+7C>T rs76114420
NM_022124.6(CDH23):c.9320-34C>T

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