NM_206933.4(USH2A):c.7584C>T (p.Thr2528=) AND not specified
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Mar 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000041911.13
Allele description [Variation Report for NM_206933.4(USH2A):c.7584C>T (p.Thr2528=)]
NM_206933.4(USH2A):c.7584C>T (p.Thr2528=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024