NM_000141.5(FGFR2):c.943G>T (p.Ala315Ser) AND not provided
- Germline classification:
- Pathogenic (3 submissions)
- Last evaluated:
- Sep 15, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001280733.7
Allele description [Variation Report for NM_000141.5(FGFR2):c.943G>T (p.Ala315Ser)]
NM_000141.5(FGFR2):c.943G>T (p.Ala315Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024