NM_006269.2(RP1):c.4112A>T (p.Asp1371Val) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 18, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001035183.7
Allele description [Variation Report for NM_006269.2(RP1):c.4112A>T (p.Asp1371Val)]
NM_006269.2(RP1):c.4112A>T (p.Asp1371Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024