NM_003799.3(RNMT):c.62C>T (p.Ser21Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 20, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004446851.1
Allele description [Variation Report for NM_003799.3(RNMT):c.62C>T (p.Ser21Leu)]
NM_003799.3(RNMT):c.62C>T (p.Ser21Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Retinoblastoma
RetinoblastomaA malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or inf...<br/>MeSH
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Last Updated: May 7, 2024