FERMT2[gene] and "single gene"[properties] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2525791	NM_006832.3(FERMT2):c.1982A>G (p.Lys661Arg)	FERMT2 (K661R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602776	NM_006832.3(FERMT2):c.1784G>T (p.Arg595Leu)	FERMT2 (R595L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478246	NM_006832.3(FERMT2):c.1718T>C (p.Phe573Ser)	FERMT2 (F573S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400674	NM_006832.3(FERMT2):c.1603-560A>G	FERMT2 (I538V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3278523	NM_006832.3(FERMT2):c.1603-566G>C	FERMT2 (G536R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2326020	NM_006832.3(FERMT2):c.1481C>G (p.Ser494Cys)	FERMT2 (S494C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257323	NM_006832.3(FERMT2):c.1442C>T (p.Ala481Val)	FERMT2 (A481V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278522	NM_006832.3(FERMT2):c.1381G>A (p.Glu461Lys)	FERMT2 (E461K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317736	NM_006832.3(FERMT2):c.1304C>T (p.Ser435Leu)	FERMT2 (S435L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408713	NM_006832.3(FERMT2):c.1271G>A (p.Arg424Lys)	FERMT2 (R424K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298709	NM_006832.3(FERMT2):c.1217G>A (p.Cys406Tyr)	FERMT2 (C406Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287169	NM_006832.3(FERMT2):c.1079G>T (p.Gly360Val)	FERMT2 (G360V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2644241	NM_006832.3(FERMT2):c.1077G>C (p.Gly359=)	FERMT2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2528250	NM_006832.3(FERMT2):c.893C>G (p.Ala298Gly)	FERMT2 (A298G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514728	NM_006832.3(FERMT2):c.658A>G (p.Ile220Val)	FERMT2 (I220V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602375	NM_006832.3(FERMT2):c.587A>G (p.His196Arg)	FERMT2 (H196R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310686	NM_006832.3(FERMT2):c.563C>G (p.Thr188Arg)	FERMT2 (T188R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284581	NM_006832.3(FERMT2):c.512T>C (p.Ile171Thr)	FERMT2 (I171T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094467	NM_006832.3(FERMT2):c.460A>C (p.Lys154Gln)	FERMT2 (K154Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353011	NM_006832.3(FERMT2):c.402C>A (p.His134Gln)	FERMT2 (H134Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364832	NM_006832.3(FERMT2):c.380G>C (p.Cys127Ser)	FERMT2 (C127S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602794	NM_006832.3(FERMT2):c.295C>G (p.Leu99Val)	FERMT2 (L99V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394212	NM_006832.3(FERMT2):c.67C>T (p.His23Tyr)	FERMT2 (H23Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357894	NM_006832.3(FERMT2):c.62G>C (p.Ser21Thr)	FERMT2 (S21T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094466	NM_006832.3(FERMT2):c.26C>T (p.Pro9Leu)	FERMT2 (P9L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360888	NM_006832.3(FERMT2):c.25C>T (p.Pro9Ser)	FERMT2 (P9S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 26