Related gene-specific medical variations for Gene (Select 25900) - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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
Select item 3108096	NM_001193457.2(IFFO1):c.194C>A (p.Ala65Asp)	IFFO1, LOC130007253 (A65D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3108095	NM_001193457.2(IFFO1):c.176C>T (p.Ala59Val)	IFFO1, LOC130007253 (A59V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3108092	NM_001193457.2(IFFO1):c.139G>C (p.Gly47Arg)	IFFO1, LOC130007253 (G47R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3108091	NM_001193457.2(IFFO1):c.139G>A (p.Gly47Ser)	IFFO1, LOC130007253 (G47S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
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 2529557	NM_001193457.2(IFFO1):c.115C>T (p.Pro39Ser)	IFFO1, LOC130007253 (P39S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471236	NM_001193457.2(IFFO1):c.163G>A (p.Gly55Arg)	IFFO1, LOC130007253 (G55R)	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 2376631	NM_001193457.2(IFFO1):c.1631C>T (p.Ala544Val)	IFFO1, LOC130007250 (A534V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363362	NM_001193457.2(IFFO1):c.104G>A (p.Gly35Glu)	IFFO1, LOC130007253 (G35E)	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 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 2249115	NM_001193457.2(IFFO1):c.452C>T (p.Pro151Leu)	IFFO1, LOC130007252 (P151L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance