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

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1765416	NM_144573.4(NEXN):c.8A>T (p.Asp3Val)	NEXN (D3V)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1315130	NM_144573.4(NEXN):c.185T>A (p.Ile62Asn)	NEXN (I62N)	Single nucleotide variant (missense variant +1 more)	NEXN-related condition +2 more	GUncertain significance
Select item 178102	NM_144573.4(NEXN):c.249G>A (p.Glu83=)	NEXN	Single nucleotide variant (synonymous variant)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 241867	NM_144573.4(NEXN):c.688-10G>A	NEXN	Single nucleotide variant (intron variant)	NEXN-related condition +4 more	GLikely benign
Select item 47910	NM_144573.4(NEXN):c.732C>A (p.Pro244=)	NEXN	Single nucleotide variant (synonymous variant)	NEXN-related condition +5 more	GBenign/Likely benign
Select item 47911	NM_144573.4(NEXN):c.733G>A (p.Gly245Arg)	NEXN (G245R +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign
Select item 30994	NM_144573.4(NEXN):c.835C>T (p.Arg279Cys)	NEXN (R279C +1 more)	Single nucleotide variant (missense variant)	not provided +6 more	GConflicting classifications of pathogenicity
Select item 47913	NM_144573.4(NEXN):c.864+12T>A	NEXN	Single nucleotide variant (intron variant)	NEXN-related condition +3 more	GBenign/Likely benign
Select item 47886	NM_144573.4(NEXN):c.1053+1G>A	NEXN	Single nucleotide variant (splice donor variant)	NEXN-related condition +7 more	GConflicting classifications of pathogenicity
Select item 2929299	NM_144573.4(NEXN):c.1231C>T (p.Leu411=)	NEXN	Single nucleotide variant (synonymous variant)	NEXN-related condition +2 more	GLikely benign
Select item 178878	NM_144573.4(NEXN):c.1252-10T>G	NEXN	Single nucleotide variant (intron variant)	NEXN-related condition +5 more	GBenign/Likely benign
Select item 2633553	NM_144573.4(NEXN):c.1292_1293del (p.Glu430_Tyr431insTer)	NEXN	Microsatellite (frameshift variant +1 more)	NEXN-related condition	GUncertain significance
Select item 47889	NM_144573.4(NEXN):c.1368A>C (p.Gly456=)	NEXN	Single nucleotide variant (synonymous variant)	NEXN-related condition +5 more	GLikely benign
Select item 1101985	NM_144573.4(NEXN):c.1419A>G (p.Arg473=)	NEXN	Single nucleotide variant (synonymous variant)	NEXN-related condition +3 more	GLikely benign
Select item 382668	NM_144573.4(NEXN):c.1488T>C (p.Asp496=)	NEXN	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 20 +4 more	GLikely benign
Select item 1773796	NM_144573.4(NEXN):c.1491T>C (p.Val497=)	NEXN	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 180456	NM_144573.4(NEXN):c.1582G>C (p.Glu528Gln)	NEXN (E528Q +1 more)	Single nucleotide variant (missense variant)	not specified +6 more	GLikely benign
Select item 47893	NM_144573.4(NEXN):c.1671GGA[2] (p.Glu561_Glu562del)	NEXN	Microsatellite (inframe_deletion)	NEXN-related condition +7 more	GConflicting classifications of pathogenicity
Select item 2633687	NM_144573.4(NEXN):c.1898G>A (p.Arg633Lys)	NEXN (R569K +1 more)	Single nucleotide variant (missense variant)	NEXN-related condition	GUncertain significance
Select item 1118356	NM_144573.4(NEXN):c.1995T>C (p.Ser665=)	NEXN	Single nucleotide variant (synonymous variant)	Cardiomyopathy +3 more	GLikely benign

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Items: 20