"PreventionGenetics, part of Exact Sciences"[submitter] AND "ZNF142"[g - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1254978	NM_001379659.1(ZNF142):c.5613G>A (p.Glu1871=)	ZNF142	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1675839	NM_001379659.1(ZNF142):c.5116C>T (p.Arg1706Trp)	ZNF142 (R1343W +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GLikely benign
Select item 3042245	NM_001379659.1(ZNF142):c.4673C>T (p.Ala1558Val)	ZNF142 (A1195V +2 more)	Single nucleotide variant (missense variant)	ZNF142-related disorder	GBenign
Select item 3036839	NM_001379659.1(ZNF142):c.4673C>A (p.Ala1558Asp)	ZNF142 (A1195D +2 more)	Single nucleotide variant (missense variant)	ZNF142-related disorder	GLikely benign
Select item 1279127	NM_001379659.1(ZNF142):c.4537G>A (p.Ala1513Thr)	ZNF142 (A1150T +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3033856	NM_001379659.1(ZNF142):c.4308G>A (p.Thr1436=)	ZNF142	Single nucleotide variant (synonymous variant)	ZNF142-related disorder	GBenign
Select item 3055973	NM_001379659.1(ZNF142):c.4173G>A (p.Arg1391=)	ZNF142	Single nucleotide variant (synonymous variant)	ZNF142-related disorder	GBenign
Select item 1241508	NM_001379659.1(ZNF142):c.3628T>C (p.Ser1210Pro)	ZNF142 (S1010P +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1290612	NM_001379659.1(ZNF142):c.3576C>A (p.Pro1192=)	ZNF142	Single nucleotide variant (synonymous variant)	ZNF142-related disorder +1 more	GBenign
Select item 1272225	NM_001379659.1(ZNF142):c.3552C>T (p.Val1184=)	ZNF142	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1288928	NM_001379659.1(ZNF142):c.3467T>A (p.Leu1156His)	ZNF142 (L1156H +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2571120	NM_001379659.1(ZNF142):c.3105C>T (p.Ala1035=)	ZNF142	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1266001	NM_001379659.1(ZNF142):c.2851A>G (p.Ser951Gly)	ZNF142 (S588G +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 1265574	NM_001379659.1(ZNF142):c.2221G>T (p.Ala741Ser)	ZNF142 (A378S +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 3045260	NM_001379659.1(ZNF142):c.1833C>T (p.Ala611=)	ZNF142	Single nucleotide variant (synonymous variant)	ZNF142-related disorder	GLikely benign
Select item 1695004	NM_001379659.1(ZNF142):c.1556G>A (p.Arg519His)	ZNF142 (R156H +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1281759	NM_001379659.1(ZNF142):c.1449A>G (p.Pro483=)	ZNF142	Single nucleotide variant (synonymous variant)	ZNF142-related disorder +1 more	GBenign
Select item 1176420	NM_001379659.1(ZNF142):c.1284G>A (p.Ala428=)	ZNF142	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3048809	NM_001379659.1(ZNF142):c.1027C>A (p.Gln343Lys)	ZNF142 (Q143K +1 more)	Single nucleotide variant (missense variant +1 more)	ZNF142-related disorder	GBenign
Select item 3056705	NM_001379659.1(ZNF142):c.1021A>C (p.Lys341Gln)	ZNF142 (K141Q +1 more)	Single nucleotide variant (missense variant +1 more)	ZNF142-related disorder	GBenign
Select item 1675840	NM_001379659.1(ZNF142):c.945G>A (p.Gln315=)	ZNF142	Single nucleotide variant (synonymous variant +1 more)	ZNF142-related disorder +1 more	GLikely benign
Select item 2651895	NM_001379659.1(ZNF142):c.510A>G (p.Arg170=)	ZNF142	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3059733	NM_001379659.1(ZNF142):c.420T>C (p.Ser140=)	ZNF142	Single nucleotide variant (synonymous variant +1 more)	ZNF142-related disorder	GBenign
Select item 2571121	NM_001379659.1(ZNF142):c.336C>T (p.Phe112=)	ZNF142	Single nucleotide variant (synonymous variant +1 more)	ZNF142-related disorder +1 more	GLikely benign
Select item 1288603	NM_001379659.1(ZNF142):c.258A>G (p.Pro86=)	ZNF142	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 2498863	NM_001379659.1(ZNF142):c.43G>A (p.Gly15Arg)	ZNF142 (G15R)	Single nucleotide variant (missense variant +1 more)	ZNF142-related disorder +1 more	GBenign/Likely benign

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Items: 26