"Ambry Genetics"[submitter] AND "SDCBP"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2522334	NM_005625.4(SDCBP):c.127G>A (p.Gly43Arg)	SDCBP (G64R +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2215297	NM_005625.4(SDCBP):c.209T>G (p.Val70Gly)	SDCBP (V64G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316790	NM_005625.4(SDCBP):c.214G>A (p.Val72Met)	SDCBP (V92M +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2244555	NM_005625.4(SDCBP):c.286G>T (p.Val96Leu)	SDCBP (V116L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3158879	NM_005625.4(SDCBP):c.362A>G (p.Gln121Arg)	SDCBP (Q120R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526630	NM_005625.4(SDCBP):c.425A>G (p.Gln142Arg)	SDCBP (Q141R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158880	NM_005625.4(SDCBP):c.590G>A (p.Arg197Gln)	SDCBP (R138Q +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158882	NM_005625.4(SDCBP):c.861G>C (p.Met287Ile)	SDCBP (M286I +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158883	NM_005625.4(SDCBP):c.866G>A (p.Ser289Asn)	SDCBP (S288N +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance