Related gene-specific medical variations for Gene (Select 11149) - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2688692	NM_001199563.2(BVES):c.937A>G (p.Thr313Ala)	BVES (T313A)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439607	NM_001199563.2(BVES):c.467A>G (p.Lys156Arg)	BVES (K156R)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439606	NM_001199563.2(BVES):c.931C>T (p.Arg311Trp)	BVES (R311W)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439605	NM_001199563.2(BVES):c.199A>G (p.Ile67Val)	BVES (I67V)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439602	NM_001199563.2(BVES):c.932G>A (p.Arg311Gln)	BVES (R311Q)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439601	NM_001199563.2(BVES):c.841C>G (p.Leu281Val)	BVES (L281V)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439600	NM_001199563.2(BVES):c.876G>A (p.Met292Ile)	BVES (M292I)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439599	NM_001199563.2(BVES):c.64G>C (p.Glu22Gln)	BVES (E22Q)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439597	NM_001199563.2(BVES):c.569T>C (p.Leu190Pro)	BVES (L190P)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439596	NM_001199563.2(BVES):c.1033G>A (p.Val345Ile)	BVES (V345I)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439594	NM_001199563.2(BVES):c.771C>G (p.Ile257Met)	BVES (I257M)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439593	NM_001199563.2(BVES):c.938C>T (p.Thr313Ile)	BVES (T313I)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439592	NM_001199563.2(BVES):c.1073A>G (p.Gln358Arg)	BVES (Q358R)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439591	NM_001199563.2(BVES):c.758T>C (p.Ile253Thr)	BVES (I253T)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439590	NM_001199563.2(BVES):c.244G>A (p.Val82Ile)	BVES (V82I)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439588	NM_001199563.2(BVES):c.938_939insT (p.Ser314fs)	BVES (S314fs)	Insertion (frameshift variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439587	NM_001199563.2(BVES):c.74T>C (p.Ile25Thr)	BVES (I25T)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439586	NM_001199563.2(BVES):c.807A>T (p.Leu269Phe)	BVES (L269F)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 2439584	NM_001199563.2(BVES):c.572A>G (p.His191Arg)	BVES (H191R)	Single nucleotide variant (missense variant)	Autosomal recessive limb-girdle muscular dystrophy type 2X	GUncertain significance
Select item 377143	NM_001199563.2(BVES):c.731_734del (p.Phe244fs)	BVES (F244fs)	Deletion (frameshift variant)	not provided	GLikely pathogenic

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Items: 20