BTF3L4[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2261562	NM_152265.5(BTF3L4):c.19G>A (p.Ala7Thr)	BTF3L4 (A7T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3135474	NM_152265.5(BTF3L4):c.37G>T (p.Val13Phe)	BTF3L4 (V13F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540395	NM_152265.5(BTF3L4):c.200T>C (p.Ile67Thr)	BTF3L4 (I9T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2405154	NM_152265.5(BTF3L4):c.257C>T (p.Thr86Ile)	BTF3L4 (T86I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2551166	NM_152265.5(BTF3L4):c.364C>T (p.Arg122Trp)	BTF3L4 (R64W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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