NM_001201543.2(FAM161A):c.1356A>G (p.Thr452=) AND Retinitis pigmentosa 28
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 21, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001279506.1
Allele description [Variation Report for NM_001201543.2(FAM161A):c.1356A>G (p.Thr452=)]
NM_001201543.2(FAM161A):c.1356A>G (p.Thr452=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024