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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH14
(G164A)
Single nucleotide variant
(missense variant)
Autosomal dominant nonsyndromic hearing loss 4A
GUncertain significance
MYH14
(S665L)
Single nucleotide variant
(missense variant +1 more)
Autosomal dominant nonsyndromic hearing loss 4A
+2 more
GConflicting classifications of pathogenicity
MYH14
(A770V +2 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
MYH14
(R947C +2 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
MYH14
(T926M +2 more)
Single nucleotide variant
(missense variant)
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome
+2 more
GConflicting classifications of pathogenicity
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