C11orf24[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2348859	NM_022338.4(C11orf24):c.964C>G (p.Pro322Ala)	C11orf24 (P322A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244098	NM_022338.4(C11orf24):c.527G>A (p.Arg176Gln)	C11orf24 (R176Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2378429	NM_022338.4(C11orf24):c.526C>T (p.Arg176Trp)	C11orf24 (R176W)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2642040	NM_022338.4(C11orf24):c.366G>A (p.Ala122=)	C11orf24	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

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