"Ambry Genetics"[submitter] AND "LPGAT1"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2556540	NM_014873.3(LPGAT1):c.1097A>G (p.Tyr366Cys)	LPGAT1 (Y399C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591478	NM_014873.3(LPGAT1):c.1083C>G (p.Ile361Met)	LPGAT1 (I361M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494398	NM_014873.3(LPGAT1):c.1064G>T (p.Gly355Val)	LPGAT1 (G355V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336954	NM_014873.3(LPGAT1):c.977C>G (p.Ser326Cys)	LPGAT1 (S359C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119752	NM_014873.3(LPGAT1):c.893A>G (p.Asp298Gly)	LPGAT1 (D331G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611760	NM_014873.3(LPGAT1):c.872A>G (p.Asp291Gly)	LPGAT1 (D291G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291171	NM_014873.3(LPGAT1):c.589G>C (p.Ala197Pro)	LPGAT1 (A197P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252881	NM_014873.3(LPGAT1):c.581C>T (p.Thr194Ile)	LPGAT1 (T194I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608833	NM_014873.3(LPGAT1):c.295G>C (p.Val99Leu)	LPGAT1 (V99L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance