Related gene-specific medical variations for Gene (Select 266675) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3260814	NM_153274.3(BEST4):c.1391C>T (p.Ala464Val)	BEST4, LOC129930423 (A464V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524063	NM_153274.3(BEST4):c.1159G>A (p.Asp387Asn)	BEST4, LOC129930423 (D387N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474436	NM_153274.3(BEST4):c.1174C>A (p.Leu392Met)	BEST4, LOC129930423 (L392M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344861	NM_153274.3(BEST4):c.1318C>G (p.Pro440Ala)	BEST4, LOC129930423 (P440A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290791	NM_153274.3(BEST4):c.1213C>A (p.Pro405Thr)	BEST4, LOC129930423 (P405T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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