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Items: 86

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYO15A
Deletion
(inframe_deletion)
not provided
GUncertain significance
MYO15A
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GConflicting classifications of pathogenicity
MYO15A
(M90T)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
MYO15A
(T132A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO15A
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
MYO15A
(D244N)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 3
+1 more
GConflicting classifications of pathogenicity
MYO15A
(G275R)
Single nucleotide variant
(missense variant)
MYO15A-related condition
+3 more
GConflicting classifications of pathogenicity
MYO15A
Single nucleotide variant
(synonymous variant)
MYO15A-related condition
+1 more
GConflicting classifications of pathogenicity
MYO15A
(D293N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
MYO15A
(D311A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO15A
(Y380fs)
Deletion
(frameshift variant)
Nonsyndromic genetic hearing loss
GLikely pathogenic
MYO15A
(Y399C)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
MYO15A
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
MYO15A
(G462D)
Single nucleotide variant
(missense variant)
MYO15A-related condition
+3 more
GBenign/Likely benign
MYO15A
(S472T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
MYO15A
(V485A)
Single nucleotide variant
(missense variant)
Cleft palate
+13 more
GConflicting classifications of pathogenicity
MYO15A
(E518K)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
MYO15A
(A595T)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign
MYO15A
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
MYO15A
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
MYO15A
(W718G)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
MYO15A
(P732S)
Single nucleotide variant
(missense variant)
MYO15A-related condition
+2 more
GConflicting classifications of pathogenicity
MYO15A
(R742L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
MYO15A
(R746S)
Single nucleotide variant
(missense variant)
Nonsyndromic genetic hearing loss
GBenign
MYO15A
(A753fs)
Deletion
(frameshift variant)
not provided
GPathogenic
MYO15A
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GConflicting classifications of pathogenicity
MYO15A
(Q821P)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
MYO15A
(E877*)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic/Likely pathogenic
MYO15A
(P894S)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
MYO15A
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GConflicting classifications of pathogenicity
MYO15A
(T1008S)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 3
+2 more
GConflicting classifications of pathogenicity
MYO15A
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
MYO15A
(R1169*)
Single nucleotide variant
(nonsense)
MYO15A-related condition
+1 more
GPathogenic
MYO15A
(R1216C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
MYO15A
(G1220E)
Single nucleotide variant
(missense variant)
MYO15A-related condition
+3 more
GConflicting classifications of pathogenicity
MYO15A
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GConflicting classifications of pathogenicity
MYO15A
(G1281R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
MYO15A
Single nucleotide variant
(splice donor variant)
not provided
+1 more
GPathogenic/Likely pathogenic
MYO15A
(R1330H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO15A
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GConflicting classifications of pathogenicity
MYO15A
(I1345L)
Single nucleotide variant
(missense variant)
MYO15A-related condition
+3 more
GConflicting classifications of pathogenicity
MYO15A
(V1400L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO15A
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
MYO15A
(A1548T)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
MYO15A
Single nucleotide variant
(intron variant)
MYO15A-related condition
+3 more
GConflicting classifications of pathogenicity
MYO15A
(R1630C)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
MYO15A
(Q1664K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO15A
(P1687L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
MYO15A
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
MYO15A
(A1772V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO15A
(L1884Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO15A
(R1956W)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
MYO15A
(C1977R)
Single nucleotide variant
(missense variant)
Nonsyndromic genetic hearing loss
GBenign
MYO15A
Single nucleotide variant
(splice acceptor variant)
not provided
GPathogenic
MYO15A
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GConflicting classifications of pathogenicity
MYO15A
(A2085T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO15A
Single nucleotide variant
(synonymous variant)
Autosomal recessive nonsyndromic hearing loss 3
+1 more
GConflicting classifications of pathogenicity
MYO15A
(T2205I)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
MYO15A
(P2208L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
MYO15A
(E2212K)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
MYO15A
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
MYO15A
Single nucleotide variant
(splice donor variant)
Autosomal recessive nonsyndromic hearing loss 3
+2 more
GConflicting classifications of pathogenicity
MYO15A
(R2262H)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
MYO15A
(V2266M)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
MYO15A
(G2357S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GConflicting classifications of pathogenicity
MYO15A
Single nucleotide variant
(synonymous variant)
Autosomal recessive nonsyndromic hearing loss 3
+1 more
GConflicting classifications of pathogenicity
MYO15A
(R2515H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO15A
(A2613D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO15A
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
MYO15A
(L2662V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+4 more
GConflicting classifications of pathogenicity
MYO15A
(L2712I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO15A
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
MYO15A
(G2930V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO15A
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
MYO15A
(E3061K)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
MYO15A
(V3108I)
Single nucleotide variant
(missense variant)
MYO15A-related condition
+3 more
GConflicting classifications of pathogenicity
MYO15A
(L3160F)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
MYO15A
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
MYO15A
Single nucleotide variant
(intron variant)
Autosomal recessive nonsyndromic hearing loss 3
+2 more
GConflicting classifications of pathogenicity
MYO15A
(Q3180R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO15A
Single nucleotide variant
(intron variant)
MYO15A-related condition
+3 more
GConflicting classifications of pathogenicity
MYO15A
(N3252D)
Single nucleotide variant
(missense variant)
MYO15A-related condition
+4 more
GConflicting classifications of pathogenicity
MYO15A
Single nucleotide variant
(synonymous variant)
MYO15A-related condition
+3 more
GConflicting classifications of pathogenicity
MYO15A
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GConflicting classifications of pathogenicity
MYO15A
(N3438D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYO15A
(S3525G)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 3
+2 more
GBenign/Likely benign
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