"Ambry Genetics"[submitter] AND "LOC130007252"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2623709	NM_001193457.2(IFFO1):c.533C>T (p.Ser178Phe)	IFFO1, LOC130007252 (S178F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3108100	NM_001193457.2(IFFO1):c.505C>T (p.Pro169Ser)	IFFO1, LOC130007252 (P169S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406955	NM_001193457.2(IFFO1):c.503C>G (p.Ala168Gly)	IFFO1, LOC130007252 (A168G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2357578	NM_001193457.2(IFFO1):c.479C>T (p.Ala160Val)	IFFO1, LOC130007252 (A160V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249115	NM_001193457.2(IFFO1):c.452C>T (p.Pro151Leu)	IFFO1, LOC130007252 (P151L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2338385	NM_001193457.2(IFFO1):c.434C>G (p.Pro145Arg)	IFFO1, LOC130007252 (P145R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3108098	NM_001193457.2(IFFO1):c.428C>T (p.Ala143Val)	IFFO1, LOC130007252 (A143V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3108097	NM_001193457.2(IFFO1):c.404G>A (p.Arg135Gln)	IFFO1, LOC130007252 (R135Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance