"Ambry Genetics"[submitter] AND "IFITM2"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3108211	NM_006435.3(IFITM2):c.22T>A (p.Phe8Ile)	IFITM2, LOC130005047 (F8I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273568	NM_006435.3(IFITM2):c.22T>C (p.Phe8Leu)	IFITM2, LOC130005047 (F8L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108212	NM_006435.3(IFITM2):c.78G>C (p.Gln26His)	IFITM2, LOC130005047 (Q26H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3108213	NM_006435.3(IFITM2):c.97G>A (p.Val33Met)	IFITM2, LOC130005047 (V33M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557722	NM_006435.3(IFITM2):c.103C>T (p.His35Tyr)	IFITM2, LOC130005047 (H35Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284375	NM_006435.3(IFITM2):c.123G>A (p.Met41Ile)	IFITM2, LOC130005047 (M41I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108210	NM_006435.3(IFITM2):c.148G>A (p.Glu50Lys)	IFITM2, LOC130005047 (E50K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235869	NM_006435.3(IFITM2):c.199A>G (p.Met67Val)	IFITM2, LOC130005047 (M67V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518760	NM_006435.3(IFITM2):c.241G>A (p.Val81Met)	IFITM2, LOC130005047 (V81M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606035	NM_006435.3(IFITM2):c.275T>C (p.Val92Ala)	IFITM2, LOC130005049 (V92A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285337	NM_006435.3(IFITM2):c.348G>A (p.Met116Ile)	IFITM2, LOC130005049 (M116I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510607	NM_006435.3(IFITM2):c.367A>C (p.Ile123Leu)	IFITM2, LOC130005049 (I123L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285339	NM_006435.3(IFITM2):c.374T>C (p.Val125Ala)	IFITM2, LOC130005049 (V125A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285338	NM_006435.3(IFITM2):c.374T>A (p.Val125Glu)	IFITM2, LOC130005049 (V125E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355543	NM_006435.3(IFITM2):c.382G>A (p.Val128Ile)	IFITM2, LOC130005049 (V128I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341040	NM_006435.3(IFITM2):c.382G>C (p.Val128Leu)	IFITM2, LOC130005049 (V128L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468693	NM_006435.3(IFITM2):c.395G>A (p.Arg132Gln)	IFITM2, LOC130005049 (R132Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance