NM_001146079.2(CLDN14):c.129C>T (p.Ala43=) AND Autosomal recessive nonsyndromic hearing loss 29
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001143199.4
Allele description [Variation Report for NM_001146079.2(CLDN14):c.129C>T (p.Ala43=)]
NM_001146079.2(CLDN14):c.129C>T (p.Ala43=)
Condition(s)
-
b5362450-2718-4f8e-8e46-9262c38cf2b4-erga
b5362450-2718-4f8e-8e46-9262c38cf2b4-ergabiosample
-
MTERFD1 AND (alive[prop]) (90)
Gene
-
ZFYVE19 zinc finger FYVE-type containing 19 [Homo sapiens]
ZFYVE19 zinc finger FYVE-type containing 19 [Homo sapiens]Gene ID:84936Gene
-
84936[uid] AND (alive[prop]) (1)
Gene
-
NCAPH AND (alive[prop]) (979)
Gene
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Last Updated: Feb 20, 2024