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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC112577517, TOR1AIP1
(G3S)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2Y
GUncertain significance
LOC112577517, TOR1AIP1
(D4G)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2Y
GUncertain significance
LOC112577517, TOR1AIP1
(R22K)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2Y
GUncertain significance
LOC112577517, TOR1AIP1
(Q52L)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2Y
+1 more
GConflicting classifications of pathogenicity
LOC112577517, TOR1AIP1
(S102N)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2Y
GUncertain significance
TOR1AIP1, LOC112577517
(R109K)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2Y
GUncertain significance
LOC112577517, TOR1AIP1
(Q117H)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2Y
GUncertain significance
LOC112577517, TOR1AIP1
(T124M)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2Y
GUncertain significance
LOC112577517, TOR1AIP1
(R125G)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2Y
+1 more
GUncertain significance
LOC112577517, TOR1AIP1
(S135L)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2Y
+2 more
GUncertain significance
LOC112577517, TOR1AIP1
(R152Q)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2Y
GUncertain significance
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