"PreventionGenetics, part of Exact Sciences"[submitter] AND "ZNF143"[g - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3031944	NM_003442.6(ZNF143):c.206-4A>C	ZNF143	Single nucleotide variant (intron variant)	ZNF143-related disorder	GLikely benign
Select item 768424	NM_003442.6(ZNF143):c.570+5A>G	ZNF143	Single nucleotide variant (intron variant)	ZNF143-related disorder +1 more	GBenign
Select item 1583011	NM_003442.6(ZNF143):c.570+7C>T	ZNF143	Single nucleotide variant (intron variant)	ZNF143-related disorder +1 more	GBenign
Select item 1280956	NM_003442.6(ZNF143):c.646-7T>C	ZNF143	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 787374	NM_003442.6(ZNF143):c.918A>G (p.Lys306=)	ZNF143	Single nucleotide variant (synonymous variant)	ZNF143-related disorder +1 more	GBenign
Select item 2065768	NM_003442.6(ZNF143):c.967+8T>C	ZNF143	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 768425	NM_003442.6(ZNF143):c.1382G>A (p.Gly461Asp)	ZNF143 (G430D +2 more)	Single nucleotide variant (missense variant)	ZNF143-related disorder +1 more	GBenign
Select item 1588196	NM_003442.6(ZNF143):c.1484G>A (p.Ser495Asn)	ZNF143 (S464N +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1288298	NM_003442.6(ZNF143):c.1681G>C (p.Glu561Gln)	ZNF143 (E530Q +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1530721	NM_003442.6(ZNF143):c.1686+8C>G	ZNF143	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1232509	NM_003442.6(ZNF143):c.1899G>A (p.Thr633=)	ZNF143	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign