NM_206933.4(USH2A):c.3800C>T (p.Ala1267Val) AND Usher syndrome type 2A
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 10, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001828683.1
Allele description [Variation Report for NM_206933.4(USH2A):c.3800C>T (p.Ala1267Val)]
NM_206933.4(USH2A):c.3800C>T (p.Ala1267Val)
Condition(s)
-
Homo sapiens cDNA clone IMAGE:9051927
Homo sapiens cDNA clone IMAGE:9051927gi|219517831|gb|BC143419.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024