NM_005170.3(ASCL2):c.237C>A (p.His79Gln) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004199383.1
Allele description [Variation Report for NM_005170.3(ASCL2):c.237C>A (p.His79Gln)]
NM_005170.3(ASCL2):c.237C>A (p.His79Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
eggcsite.comN5Y (0)
BioProject
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Jun 9, 2024