NM_000260.4(MYO7A):c.3527G>A (p.Ser1176Asn) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002500491.1
Allele description [Variation Report for NM_000260.4(MYO7A):c.3527G>A (p.Ser1176Asn)]
NM_000260.4(MYO7A):c.3527G>A (p.Ser1176Asn)
Condition(s)
- Name:
- Autosomal dominant nonsyndromic hearing loss 11
- Synonyms:
- Deafness, autosomal dominant 11
- Identifiers:
- MONDO: MONDO:0011032; MedGen: C1832475; Orphanet: 90635; OMIM: 601317
-
S41 family peptidase [Rhizobium croatiense]
S41 family peptidase [Rhizobium croatiense]gi|2463813653|gnl|PRJNA939359|PYR68 0|gb|WET73573.1|Protein
-
S41 family peptidase [Algibacter luteus]
S41 family peptidase [Algibacter luteus]gi|2524566253|gnl|PRJNA914060|O5O44 5|gb|WJJ97035.1|Protein
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Last Updated: Oct 13, 2024