NM_213647.3(FGFR4):c.409T>C (p.Ser137Pro) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 17, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004394150.1
Allele description [Variation Report for NM_213647.3(FGFR4):c.409T>C (p.Ser137Pro)]
NM_213647.3(FGFR4):c.409T>C (p.Ser137Pro)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024