NM_206933.4(USH2A):c.10896C>T (p.Leu3632=) AND Retinitis pigmentosa 39
- Germline classification:
- Likely benign (1 submission)
- 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:
- RCV003453181.1
Allele description [Variation Report for NM_206933.4(USH2A):c.10896C>T (p.Leu3632=)]
NM_206933.4(USH2A):c.10896C>T (p.Leu3632=)
Condition(s)
-
txid979557[Organism:noexp] (2)
Identical Protein Groups
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See more...Assertion and evidence details
Last Updated: Feb 28, 2024