NM_023110.3(FGFR1):c.1671G>T (p.Leu557Phe) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 16, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000722312.1
Allele description [Variation Report for NM_023110.3(FGFR1):c.1671G>T (p.Leu557Phe)]
NM_023110.3(FGFR1):c.1671G>T (p.Leu557Phe)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 23, 2022