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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBCEL-TECTA, TECTA
Single nucleotide variant
(synonymous variant)
Autosomal recessive nonsyndromic hearing loss 21
GUncertain significance
TBCEL-TECTA, TECTA
Single nucleotide variant
(synonymous variant)
Autosomal recessive nonsyndromic hearing loss 21
GUncertain significance
TECTA, TBCEL-TECTA
(G1020S +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 21
GUncertain significance
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