MEA1[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3124776	NM_014623.4(MEA1):c.533G>A (p.Arg178Gln)	MEA1 (R178Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513961	NM_014623.4(MEA1):c.532C>T (p.Arg178Trp)	MEA1 (R181W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124775	NM_014623.4(MEA1):c.455C>T (p.Ala152Val)	MEA1 (A139V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124774	NM_014623.4(MEA1):c.403C>G (p.Pro135Ala)	MEA1 (P122A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357377	NM_014623.4(MEA1):c.371C>T (p.Ala124Val)	MEA1 (A111V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656570	NM_014623.4(MEA1):c.356AGG[1] (p.Glu120del)	MEA1 (E107del +2 more)	Microsatellite (inframe_deletion)	not provided	GLikely benign
Select item 3124773	NM_014623.4(MEA1):c.357G>T (p.Glu119Asp)	MEA1 (E122D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124771	NM_014623.4(MEA1):c.296G>A (p.Arg99Gln)	MEA1 (R102Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320715	NM_014623.4(MEA1):c.260T>C (p.Val87Ala)	MEA1 (V87A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293913	NM_014623.4(MEA1):c.236A>G (p.Gln79Arg)	MEA1 (Q66R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293914	NM_014623.4(MEA1):c.229C>T (p.Pro77Ser)	MEA1 (P77S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124770	NM_014623.4(MEA1):c.182C>T (p.Thr61Met)	MEA1 (T48M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124769	NM_014623.4(MEA1):c.169G>A (p.Glu57Lys)	MEA1 (E60K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494618	NM_014623.4(MEA1):c.119A>G (p.Gln40Arg)	MEA1 (Q40R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318247	NM_014623.4(MEA1):c.89T>C (p.Phe30Ser)	MEA1 (F17S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance