"Genome-Nilou Lab"[submitter] AND "C10orf105"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 676346	NM_022124.6(CDH23):c.3370-46T>C	C10orf105, CDH23	Single nucleotide variant (intron variant)	Usher syndrome type 1D +2 more	GBenign
Select item 1177634	NM_022124.6(CDH23):c.3430+114T>C	C10orf105, CDH23	Single nucleotide variant (intron variant)	Autosomal recessive nonsyndromic hearing loss 12 +2 more	GBenign
Select item 1177635	NM_022124.6(CDH23):c.3431-205A>C	C10orf105, CDH23	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 1177636	NM_022124.6(CDH23):c.3431-133T>C	C10orf105, CDH23	Single nucleotide variant (intron variant)	Autosomal recessive nonsyndromic hearing loss 12 +2 more	GBenign/Likely benign
Select item 45927	NM_022124.6(CDH23):c.3664G>A (p.Ala1222Thr)	C10orf105, CDH23 (A1222T)	Single nucleotide variant (missense variant +1 more)	Usher syndrome type 1D +3 more	GBenign/Likely benign
Select item 45937	NM_022124.6(CDH23):c.4051A>G (p.Asn1351Asp)	C10orf105, CDH23 (N1351D)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GBenign
Select item 1195970	NM_022124.6(CDH23):c.4183G>A (p.Gly1395Ser)	C10orf105, CDH23 (G1395S)	Single nucleotide variant (missense variant +1 more)	Usher syndrome type 1D +1 more	GUncertain significance
Select item 670326	NM_022124.6(CDH23):c.4206+61T>A	C10orf105, CDH23	Single nucleotide variant (intron variant)	Usher syndrome type 1D +2 more	GBenign
Select item 678773	NM_022124.6(CDH23):c.4206+131T>C	C10orf105, CDH23	Single nucleotide variant (intron variant)	Pituitary adenoma 5, multiple types +3 more	GBenign