NM_015331.3(NCSTN):c.21C>T (p.Gly7=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003580025.2
Allele description [Variation Report for NM_015331.3(NCSTN):c.21C>T (p.Gly7=)]
NM_015331.3(NCSTN):c.21C>T (p.Gly7=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 13, 2024