FAM3A[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3092411	NM_021806.4(FAM3A):c.652G>A (p.Glu218Lys)	FAM3A (E180K +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 736968	NM_021806.4(FAM3A):c.642C>T (p.Pro214=)	FAM3A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2351164	NM_021806.4(FAM3A):c.409A>G (p.Ile137Val)	FAM3A (I137V +4 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 770831	NM_021806.4(FAM3A):c.393C>T (p.Asn131=)	FAM3A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2661849	NM_021806.4(FAM3A):c.362G>A (p.Arg121Gln)	FAM3A (R121Q +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2661850	NM_021806.4(FAM3A):c.354C>T (p.Ile118=)	FAM3A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2623379	NM_021806.4(FAM3A):c.169T>C (p.Tyr57His)	FAM3A (Y19H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092410	NM_021806.4(FAM3A):c.163A>G (p.Arg55Gly)	FAM3A (R17G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2661851	NM_021806.4(FAM3A):c.141G>A (p.Ser47=)	FAM3A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign