NM_206933.4(USH2A):c.3212A>G (p.Asn1071Ser) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jun 16, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001235728.5
Allele description [Variation Report for NM_206933.4(USH2A):c.3212A>G (p.Asn1071Ser)]
NM_206933.4(USH2A):c.3212A>G (p.Asn1071Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024