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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MRE11
(D692E +2 more)
Single nucleotide variant
(missense variant)
Ataxia-telangiectasia-like disorder 1
+2 more
GUncertain significance
MRE11
(T603A +1 more)
Single nucleotide variant
(missense variant +1 more)
Ataxia-telangiectasia-like disorder
+2 more
GUncertain significance
MRE11
Single nucleotide variant
(intron variant)
Ataxia-telangiectasia-like disorder 1
+2 more
GConflicting classifications of pathogenicity
MRE11
(R576Q)
Single nucleotide variant
(missense variant)
not specified
+9 more
GConflicting classifications of pathogenicity
MRE11
(R488C)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
MRE11
(H283R)
Single nucleotide variant
(missense variant)
Ataxia-telangiectasia-like disorder
+2 more
GUncertain significance
MRE11
(A177T)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
MRE11
(I176V)
Single nucleotide variant
(missense variant)
Ataxia-telangiectasia-like disorder
+1 more
GConflicting classifications of pathogenicity
MRE11
(S165C)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MRE11
(H152P)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MRE11
(I120V)
Single nucleotide variant
(missense variant)
Ataxia-telangiectasia-like disorder 1
+3 more
GUncertain significance
MRE11
(G102V)
Single nucleotide variant
(missense variant)
Ataxia-telangiectasia-like disorder
+1 more
GConflicting classifications of pathogenicity
MRE11
(M26V)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
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