"Ambry Genetics"[submitter] AND "ELAVL1"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2288109	NM_001419.3(ELAVL1):c.898A>T (p.Met300Leu)	ELAVL1 (M300L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088216	NM_001419.3(ELAVL1):c.827T>G (p.Ile276Ser)	ELAVL1 (I276S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088215	NM_001419.3(ELAVL1):c.772G>T (p.Gly258Trp)	ELAVL1 (G258W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088214	NM_001419.3(ELAVL1):c.538A>G (p.Thr180Ala)	ELAVL1 (T180A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088213	NM_001419.3(ELAVL1):c.392G>A (p.Arg131Gln)	ELAVL1 (R131Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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