ClinVar Miner

List of variants in gene CCDC50 reported as likely benign for not specified

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Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_178335.3(CCDC50):c.1203A>G (p.Lys401=) rs146511344 0.00163
NM_178335.3(CCDC50):c.1429+5G>A rs375535283 0.00038
NM_178335.3(CCDC50):c.113-4C>G rs145892736 0.00007
NM_178335.3(CCDC50):c.153G>A (p.Leu51=) rs201015131 0.00004
NM_178335.3(CCDC50):c.1003G>A (p.Ala335Thr) rs727502917 0.00002
NM_178335.3(CCDC50):c.136G>A (p.Val46Ile) rs762006742 0.00001
NM_178335.3(CCDC50):c.697C>G (p.Pro233Ala) rs747154818 0.00001
NM_178335.3(CCDC50):c.804G>A (p.Gln268=) rs876657435 0.00001
NM_178335.3(CCDC50):c.1231C>T (p.Pro411Ser) rs138707536
NM_178335.3(CCDC50):c.749A>G (p.Glu250Gly) rs727502916

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