NM_001265589.2(RTN3):c.1373G>A (p.Cys458Tyr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004171704.1
Allele description [Variation Report for NM_001265589.2(RTN3):c.1373G>A (p.Cys458Tyr)]
NM_001265589.2(RTN3):c.1373G>A (p.Cys458Tyr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
365 -bet365 eggc.vipGIn (0)
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Last Updated: Jun 9, 2024