NM_030662.4(MAP2K2):c.1092A>C (p.Thr364=) AND Noonan syndrome and Noonan-related syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 19, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001813551.3
Allele description [Variation Report for NM_030662.4(MAP2K2):c.1092A>C (p.Thr364=)]
NM_030662.4(MAP2K2):c.1092A>C (p.Thr364=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024