"PreventionGenetics, part of Exact Sciences"[submitter] AND "FAM47B"[g - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3035806	NM_152631.3(FAM47B):c.18A>G (p.Pro6=)	FAM47B	Single nucleotide variant (synonymous variant)	FAM47B-related condition	GLikely benign
Select item 3035472	NM_152631.3(FAM47B):c.30A>C (p.Pro10=)	FAM47B	Single nucleotide variant (synonymous variant)	FAM47B-related condition	GLikely benign
Select item 3035854	NM_152631.3(FAM47B):c.39A>G (p.Gln13=)	FAM47B	Single nucleotide variant (synonymous variant)	FAM47B-related condition	GLikely benign
Select item 3054088	NM_152631.3(FAM47B):c.329_337del (p.Val110_Pro112del)	FAM47B	Deletion (inframe deletion)	FAM47B-related condition	GLikely benign
Select item 3042837	NM_152631.3(FAM47B):c.711G>A (p.Pro237=)	FAM47B	Single nucleotide variant (synonymous variant)	FAM47B-related condition	GLikely benign
Select item 3052391	NM_152631.3(FAM47B):c.766G>T (p.Val256Leu)	FAM47B (V256L)	Single nucleotide variant (missense variant)	FAM47B-related condition	GBenign
Select item 3041116	NM_152631.3(FAM47B):c.923G>A (p.Arg308His)	FAM47B (R308H)	Single nucleotide variant (missense variant)	FAM47B-related condition	GBenign
Select item 3053834	NM_152631.3(FAM47B):c.963G>A (p.Pro321=)	FAM47B	Single nucleotide variant (synonymous variant)	FAM47B-related condition	GLikely benign
Select item 3044150	NM_152631.3(FAM47B):c.1313T>C (p.Leu438Pro)	FAM47B (L438P)	Single nucleotide variant (missense variant)	FAM47B-related condition	GBenign
Select item 3041253	NM_152631.3(FAM47B):c.1617T>C (p.Tyr539=)	FAM47B	Single nucleotide variant (synonymous variant)	FAM47B-related condition	GLikely benign
Select item 3048754	NM_152631.3(FAM47B):c.1863T>A (p.Val621=)	FAM47B	Single nucleotide variant (synonymous variant)	FAM47B-related condition	GBenign