"GeneDx"[submitter] AND "ZFP57"[gene] - ClinVar

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Search results

Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1290020	NC_000006.12:g.29672244T>C	MOG, ZFP57	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1249969	NC_000006.12:g.29672293TAAA[10]	MOG, ZFP57	Microsatellite (3 prime UTR variant)	not provided	GBenign
Select item 130773	NM_001109809.5(ZFP57):c.1103A>T (p.Asp368Val)	ZFP57 (D368V +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 130771	NM_001109809.5(ZFP57):c.593A>G (p.Asn198Ser)	ZFP57 (N198S +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign
Select item 130775	NM_001109809.5(ZFP57):c.559C>T (p.Arg187Cys)	ZFP57 (R187C +1 more)	Single nucleotide variant (missense variant)	Diabetes mellitus, transient neonatal, 1 +1 more	GBenign
Select item 1234686	NM_001109809.5(ZFP57):c.353-78C>T	ZFP57	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234971	NM_001109809.5(ZFP57):c.353-102C>T	ZFP57	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273997	NM_001109809.5(ZFP57):c.353-152T>C	ZFP57	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230106	NM_001109809.5(ZFP57):c.352+212dup	ZFP57	Indel (intron variant)	not provided	GBenign
Select item 1241635	NM_001109809.5(ZFP57):c.352+234del	ZFP57	Deletion (intron variant)	not provided	GBenign
Select item 1222615	NM_001109809.5(ZFP57):c.352+232_352+234del	ZFP57	Microsatellite (intron variant)	not provided	GBenign
Select item 1243732	NM_001109809.5(ZFP57):c.352+213T>C	ZFP57	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282811	NM_001109809.5(ZFP57):c.352+177_352+184dup	ZFP57	Microsatellite (intron variant)	not provided	GBenign
Select item 1242039	NM_001109809.5(ZFP57):c.251-23T>G	ZFP57	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249439	NM_001109809.5(ZFP57):c.250+220T>C	ZFP57	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248722	NM_001109809.5(ZFP57):c.124-41T>C	ZFP57	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241275	NM_001109809.5(ZFP57):c.124-204G>A	ZFP57	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271856	NM_001109809.5(ZFP57):c.123+156G>A	ZFP57	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281971	NM_001109809.5(ZFP57):c.123+25G>A	ZFP57	Single nucleotide variant (intron variant)	Diabetes mellitus, transient neonatal, 1 +1 more	GBenign
Select item 1279190	NM_001109809.5(ZFP57):c.-190A>G	ZFP57	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1251245	NM_001109809.5(ZFP57):c.-258G>T	ZFP57	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1179858	NM_001109809.5(ZFP57):c.-338C>G	ZFP57	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign

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Items: 22