ZNF688[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2545248	NM_145271.4(ZNF688):c.776G>A (p.Arg259Gln)	ZNF688 (R259Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296077	NM_145271.4(ZNF688):c.643G>C (p.Glu215Gln)	ZNF688 (E215Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259207	NM_145271.4(ZNF688):c.572G>A (p.Arg191His)	ZNF688 (R177H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368124	NM_145271.4(ZNF688):c.544C>A (p.Arg182Ser)	ZNF688 (R168S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197749	NM_145271.4(ZNF688):c.512T>C (p.Ile171Thr)	ZNF688 (I171T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525447	NM_145271.4(ZNF688):c.488C>T (p.Thr163Ile)	ZNF688 (T163I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348647	NM_145271.4(ZNF688):c.461C>G (p.Pro154Arg)	ZNF688 (P140R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197748	NM_145271.4(ZNF688):c.440C>T (p.Ala147Val)	ZNF688 (A147V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475704	NM_145271.4(ZNF688):c.406G>A (p.Val136Met)	ZNF688 (V136M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319229	NM_145271.4(ZNF688):c.305G>A (p.Arg102Gln)	ZNF688 (R102Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495758	NM_145271.4(ZNF688):c.246T>G (p.Ser82Arg)	ZNF688 (S82R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259208	NM_145271.4(ZNF688):c.244A>G (p.Ser82Gly)	ZNF688 (S82G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259206	NM_145271.4(ZNF688):c.239A>C (p.Gln80Pro)	ZNF688 (Q66P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance