NM_206933.4(USH2A):c.13832C>T (p.Ala4611Val) AND Usher syndrome type 2A
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Nov 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001830130.4
Allele description [Variation Report for NM_206933.4(USH2A):c.13832C>T (p.Ala4611Val)]
NM_206933.4(USH2A):c.13832C>T (p.Ala4611Val)
Condition(s)
-
Homo sapiens leucine-rich repeat kinase 1, mRNA (cDNA clone IMAGE:3463102)
Homo sapiens leucine-rich repeat kinase 1, mRNA (cDNA clone IMAGE:3463102)gi|18042971|gb|BC020379.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Dec 30, 2023