NM_001166108.2(PALLD):c.3351C>T (p.Asp1117=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 13, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004024368.1
Allele description [Variation Report for NM_001166108.2(PALLD):c.3351C>T (p.Asp1117=)]
NM_001166108.2(PALLD):c.3351C>T (p.Asp1117=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 10, 2024