NM_173630.4(RTTN):c.6038G>T (p.Cys2013Phe) AND RTTN-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 18, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003915166.1
Allele description [Variation Report for NM_173630.4(RTTN):c.6038G>T (p.Cys2013Phe)]
NM_173630.4(RTTN):c.6038G>T (p.Cys2013Phe)
Condition(s)
- Name:
- RTTN-related disorder
- Synonyms:
- RTTN-related condition
- Identifiers:
-
C4479652[trait identifier] AND "Revvity Omics, Revvity"[submitter... (5)
C4479652[trait identifier] AND "Revvity Omics, Revvity"[submitter]SearchClinVar
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Last Updated: May 19, 2024