"PreventionGenetics, part of Exact Sciences"[submitter] AND "NSD3"[gen - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3052725	NM_023034.2(NSD3):c.3798G>C (p.Leu1266=)	NSD3	Single nucleotide variant (synonymous variant)	NSD3-related condition	GLikely benign
Select item 3058261	NM_023034.2(NSD3):c.3523G>A (p.Val1175Ile)	NSD3 (V1175I)	Single nucleotide variant (missense variant)	NSD3-related condition	GLikely benign
Select item 713975	NM_023034.2(NSD3):c.2961C>T (p.Asn987=)	NSD3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3042747	NM_023034.2(NSD3):c.2262G>A (p.Ser754=)	NSD3	Single nucleotide variant (synonymous variant)	NSD3-related condition	GLikely benign
Select item 3056359	NM_023034.2(NSD3):c.1959C>T (p.Ser653=)	NSD3	Single nucleotide variant (synonymous variant)	NSD3-related condition	GLikely benign
Select item 3039064	NM_023034.2(NSD3):c.1392G>A (p.Pro464=)	NSD3	Single nucleotide variant (synonymous variant)	NSD3-related condition	GLikely benign
Select item 3035790	NM_023034.2(NSD3):c.1386G>A (p.Glu462=)	NSD3	Single nucleotide variant (synonymous variant)	NSD3-related condition	GLikely benign
Select item 3044380	NM_023034.2(NSD3):c.1314G>A (p.Val438=)	NSD3	Single nucleotide variant (synonymous variant)	NSD3-related condition	GLikely benign
Select item 3034422	NM_023034.2(NSD3):c.771T>C (p.Val257=)	LOC107133509, NSD3	Single nucleotide variant (synonymous variant)	NSD3-related condition	GLikely benign
Select item 3043083	NM_023034.2(NSD3):c.237G>T (p.Val79=)	NSD3	Single nucleotide variant (synonymous variant)	NSD3-related condition	GLikely benign