"Ambry Genetics"[submitter] AND "TAGLN2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2367729	NM_003564.3(TAGLN2):c.551C>T (p.Ala184Val)	TAGLN2 (A184V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2315273	NM_003564.3(TAGLN2):c.541A>G (p.Asn181Asp)	TAGLN2 (N202D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2530383	NM_003564.3(TAGLN2):c.476C>A (p.Pro159His)	TAGLN2 (P159H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2476959	NM_003564.3(TAGLN2):c.380G>A (p.Arg127Gln)	TAGLN2 (R148Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2455080	NM_003564.3(TAGLN2):c.255G>A (p.Met85Ile)	TAGLN2 (M106I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2619109	NM_003564.3(TAGLN2):c.253A>G (p.Met85Val)	TAGLN2 (M85V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2248549	NM_003564.3(TAGLN2):c.23A>G (p.Tyr8Cys)	TAGLN2 (Y29C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar