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

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2380909	NM_000714.6(TSPO):c.71G>A (p.Arg24His)	TSPO (R24H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183867	NM_000714.6(TSPO):c.161G>A (p.Gly54Asp)	TSPO (G54D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303667	NM_000714.6(TSPO):c.175G>A (p.Ala59Thr)	TSPO (A59T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619965	NM_000714.6(TSPO):c.215G>A (p.Gly72Glu)	TSPO (G72E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2232769	NM_000714.6(TSPO):c.295T>G (p.Phe99Val)	TSPO (F99V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2537782	NM_000714.6(TSPO):c.296T>C (p.Phe99Ser)	TSPO (F99S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527857	NM_000714.6(TSPO):c.383A>T (p.Gln128Leu)	TSPO (Q128L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3329672	NM_000714.6(TSPO):c.411C>G (p.Leu137=)	TSPO	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 2306052	NM_000714.6(TSPO):c.458G>A (p.Cys153Tyr)	TSPO (C153Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3329673	NM_000714.6(TSPO):c.476A>G (p.His159Arg)	TSPO (H159R)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign