NM_001195248.2(APTX):c.618G>T (p.Pro206=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 26, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000603717.1
Allele description
NM_001195248.2(APTX):c.618G>T (p.Pro206=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2021