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Items: 37

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OTOG
(G32S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OTOG
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
OTOG
(F214del +1 more)
Microsatellite
(inframe_deletion)
not provided
+2 more
GUncertain significance
OTOG
(P325T +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
OTOG
(R441W +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GLikely benign
OTOG
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
OTOG
(D812N +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
OTOG
(T898M +1 more)
Single nucleotide variant
(missense variant)
OTOG-related condition
+1 more
GConflicting classifications of pathogenicity
OTOG
Single nucleotide variant
(intron variant)
not provided
GConflicting classifications of pathogenicity
OTOG
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
OTOG
(R1350Q +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OTOG
(A1375P +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 18B
+2 more
GBenign
OTOG
(A1555T +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
OTOG
(T1588A +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OTOG
(R1624H +1 more)
Single nucleotide variant
(missense variant)
OTOG-related condition
+2 more
GConflicting classifications of pathogenicity
OTOG
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
OTOG
(A2037V +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 18B
+4 more
GConflicting classifications of pathogenicity
OTOG
(V2073M +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
OTOG
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
OTOG
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
OTOG
(G2204V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OTOG
(V2235M +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
OTOG
(K2239E +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OTOG
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
OTOG
(R2310H +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
OTOG
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
OTOG
Duplication
(splice acceptor variant)
not specified
+2 more
GConflicting classifications of pathogenicity
OTOG
(A2516T +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
OTOG
(R2556Q +1 more)
Single nucleotide variant
(missense variant)
Meniere disease
+2 more
GConflicting classifications of pathogenicity
OTOG
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
OTOG
Single nucleotide variant
(splice donor variant)
not specified
+2 more
GConflicting classifications of pathogenicity
OTOG
(A2593V +1 more)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
OTOG
(D2635N +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
OTOG
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
OTOG
(R2750W +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OTOG
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign/Likely benign
OTOG
(Q2900* +1 more)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
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