"Ambry Genetics"[submitter] AND "ZNF410"[gene] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2525536	NM_021188.3(ZNF410):c.77A>C (p.Gln26Pro)	ZNF410 (Q26P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2615219	NM_021188.3(ZNF410):c.82C>T (p.Leu28Phe)	ZNF410 (L28F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2488249	NM_021188.3(ZNF410):c.140C>T (p.Ala47Val)	ZNF410 (A47V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2230744	NM_021188.3(ZNF410):c.182A>G (p.Asn61Ser)	ZNF410 (N61S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2354350	NM_021188.3(ZNF410):c.235C>T (p.Arg79Trp)	ZNF410 (R79W +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2211781	NM_021188.3(ZNF410):c.242A>G (p.Asn81Ser)	ZNF410 (N81S +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3195586	NM_021188.3(ZNF410):c.293C>T (p.Pro98Leu)	ZNF410 (P98L +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3195587	NM_021188.3(ZNF410):c.322A>G (p.Ser108Gly)	ZNF410 (S108G +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2221396	NM_021188.3(ZNF410):c.434C>G (p.Ala145Gly)	ZNF410 (A145G +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2516858	NM_021188.3(ZNF410):c.541C>T (p.Arg181Cys)	ZNF410 (R198C +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2617803	NM_021188.3(ZNF410):c.593A>C (p.His198Pro)	ZNF410 (H125P +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195588	NM_021188.3(ZNF410):c.627T>C (p.Ser209=)	ZNF410 (L23P)	Single nucleotide variant (synonymous variant +2 more)	not specified	GLikely benign
Select item 2568626	NM_021188.3(ZNF410):c.631C>T (p.Pro211Ser)	ZNF410 (P228S +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2535310	NM_021188.3(ZNF410):c.632C>T (p.Pro211Leu)	ZNF410 (P228L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195589	NM_021188.3(ZNF410):c.668T>C (p.Val223Ala)	ZNF410 (V150A +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2342483	NM_021188.3(ZNF410):c.760G>A (p.Glu254Lys)	ZNF410 (E181K +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2325774	NM_021188.3(ZNF410):c.762A>T (p.Glu254Asp)	ZNF410 (E181D +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517690	NM_021188.3(ZNF410):c.991G>T (p.Val331Leu)	ZNF410 (V135L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195584	NM_021188.3(ZNF410):c.1116G>T (p.Glu372Asp)	ZNF410 (E299D +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2382605	NM_021188.3(ZNF410):c.1171G>A (p.Val391Ile)	ZNF410 (V408I +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2244563	NM_021188.3(ZNF410):c.1295G>T (p.Arg432Leu)	FAM161B, ZNF410 (R359L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213531	NM_021188.3(ZNF410):c.1295G>A (p.Arg432His)	FAM161B, ZNF410 (R236H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 22