Related gene-specific medical variations for Gene (Select 126807286) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3291160	NM_024830.5(LPCAT1):c.359G>A (p.Arg120Gln)	LOC126807286, LPCAT1 (R120Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119731	NM_024830.5(LPCAT1):c.349G>A (p.Val117Met)	LOC126807286, LPCAT1 (V117M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608497	NM_024830.5(LPCAT1):c.328G>T (p.Gly110Cys)	LOC126807286, LPCAT1 (G110C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553362	NM_024830.5(LPCAT1):c.314C>A (p.Thr105Asn)	LOC126807286, LPCAT1 (T105N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363161	NM_024830.5(LPCAT1):c.482C>T (p.Pro161Leu)	LOC126807286, LPCAT1 (P161L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216860	NM_024830.5(LPCAT1):c.302C>T (p.Ala101Val)	LOC126807286, LPCAT1 (A101V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209510	NM_024830.5(LPCAT1):c.341G>A (p.Arg114Gln)	LOC126807286, LPCAT1 (R114Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar