NM_000371.4(TTR):c.147C>T (p.Ala49=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 29, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000588441.9
Allele description [Variation Report for NM_000371.4(TTR):c.147C>T (p.Ala49=)]
NM_000371.4(TTR):c.147C>T (p.Ala49=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 26, 2024