"PreventionGenetics, part of Exact Sciences"[submitter] AND "ZNF512B"[ - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3046525	NM_020713.3(ZNF512B):c.*9C>T	ZNF512B	Single nucleotide variant (3 prime UTR variant)	ZNF512B-related disorder	GLikely benign
Select item 3059327	NM_020713.3(ZNF512B):c.2460C>T (p.Pro820=)	ZNF512B	Single nucleotide variant (synonymous variant)	ZNF512B-related disorder	GBenign
Select item 3049856	NM_020713.3(ZNF512B):c.2332G>T (p.Ala778Ser)	ZNF512B (A778S)	Single nucleotide variant (missense variant)	ZNF512B-related disorder	GLikely benign
Select item 3055650	NM_020713.3(ZNF512B):c.2187C>T (p.Leu729=)	ZNF512B	Single nucleotide variant (synonymous variant)	ZNF512B-related disorder	GBenign
Select item 3052187	NM_020713.3(ZNF512B):c.2151C>T (p.Pro717=)	ZNF512B	Single nucleotide variant (synonymous variant)	ZNF512B-related disorder	GLikely benign
Select item 3048867	NM_020713.3(ZNF512B):c.2112C>T (p.Arg704=)	ZNF512B	Single nucleotide variant (synonymous variant)	ZNF512B-related disorder	GLikely benign
Select item 3041998	NM_020713.3(ZNF512B):c.2055G>A (p.Thr685=)	ZNF512B	Single nucleotide variant (synonymous variant)	ZNF512B-related disorder	GLikely benign
Select item 3037319	NM_020713.3(ZNF512B):c.1779G>T (p.Arg593=)	ZNF512B	Single nucleotide variant (synonymous variant)	ZNF512B-related disorder	GBenign
Select item 3059781	NM_020713.3(ZNF512B):c.1578T>C (p.Leu526=)	ZNF512B	Single nucleotide variant (synonymous variant)	ZNF512B-related disorder	GBenign
Select item 3059672	NM_020713.3(ZNF512B):c.1357G>A (p.Ala453Thr)	ZNF512B (A453T)	Single nucleotide variant (missense variant)	ZNF512B-related disorder	GBenign
Select item 3039413	NM_020713.3(ZNF512B):c.1222G>A (p.Ala408Thr)	ZNF512B (A408T)	Single nucleotide variant (missense variant)	ZNF512B-related disorder	GBenign
Select item 3060619	NM_020713.3(ZNF512B):c.1114A>G (p.Met372Val)	ZNF512B (M372V)	Single nucleotide variant (missense variant)	ZNF512B-related disorder	GBenign
Select item 3035032	NM_020713.3(ZNF512B):c.957G>A (p.Pro319=)	ZNF512B	Single nucleotide variant (synonymous variant)	ZNF512B-related disorder	GBenign
Select item 3059862	NM_020713.3(ZNF512B):c.862G>A (p.Val288Met)	ZNF512B (V288M)	Single nucleotide variant (missense variant)	ZNF512B-related disorder	GBenign
Select item 3059501	NM_020713.3(ZNF512B):c.834A>C (p.Val278=)	ZNF512B	Single nucleotide variant (synonymous variant)	ZNF512B-related disorder	GBenign
Select item 3045047	NM_020713.3(ZNF512B):c.675C>T (p.Thr225=)	ZNF512B	Single nucleotide variant (synonymous variant)	ZNF512B-related disorder	GLikely benign
Select item 3049384	NM_020713.3(ZNF512B):c.576C>A (p.Ile192=)	ZNF512B	Single nucleotide variant (synonymous variant)	ZNF512B-related disorder	GLikely benign
Select item 3038137	NM_020713.3(ZNF512B):c.532A>G (p.Arg178Gly)	ZNF512B (R178G)	Single nucleotide variant (missense variant)	ZNF512B-related disorder	GLikely benign
Select item 3044196	NM_020713.3(ZNF512B):c.435C>T (p.Cys145=)	ZNF512B	Single nucleotide variant (synonymous variant)	ZNF512B-related disorder	GLikely benign
Select item 3042777	NM_020713.3(ZNF512B):c.279C>T (p.Asn93=)	ZNF512B	Single nucleotide variant (synonymous variant)	ZNF512B-related disorder	GLikely benign
Select item 3060013	NM_020713.3(ZNF512B):c.183G>A (p.Pro61=)	ZNF512B	Single nucleotide variant (synonymous variant)	ZNF512B-related disorder	GBenign

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Items: 21