NM_153676.4(USH1C):c.2401G>T (p.Glu801Ter) AND Autosomal recessive nonsyndromic hearing loss 18A
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Mar 15, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003462789.2
Allele description [Variation Report for NM_153676.4(USH1C):c.2401G>T (p.Glu801Ter)]
NM_153676.4(USH1C):c.2401G>T (p.Glu801Ter)
Condition(s)
-
Homo sapiens fer-1-like 4 (C. elegans), mRNA (cDNA clone IMAGE:5169552)
Homo sapiens fer-1-like 4 (C. elegans), mRNA (cDNA clone IMAGE:5169552)gi|20455825|gb|BC029951.1|Nucleotide
-
Rattus norvegicus spermatogenesis associated 6, mRNA (cDNA clone IMAGE:7457163),...
Rattus norvegicus spermatogenesis associated 6, mRNA (cDNA clone IMAGE:7457163), partial cdsgi|165970645|gb|BC158581.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024