ClinVar Miner

List of variants in gene CCNF, TBC1D24 studied for Developmental and epileptic encephalopathy, 1; Autosomal dominant nonsyndromic hearing loss 65; Caused by mutation in the TBC1 domain family, member 24

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001199107.2(TBC1D24):c.641G>A (p.Arg214His)	rs200324356	0.00068
NM_001199107.2(TBC1D24):c.1025C>T (p.Ser342Leu)	rs1159971280	0.00003

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