NM_023110.3(FGFR1):c.2348C>T (p.Thr783Ile) AND FGFR1-related disorder
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 22, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004539137.2
Allele description [Variation Report for NM_023110.3(FGFR1):c.2348C>T (p.Thr783Ile)]
NM_023110.3(FGFR1):c.2348C>T (p.Thr783Ile)
Condition(s)
- Name:
- FGFR1-related disorder
- Synonyms:
- FGFR1-related condition; FGFR1-Related Disorders
- Identifiers:
-
Homo sapiens cDNA clone IMAGE:4696653
Homo sapiens cDNA clone IMAGE:4696653gi|38541865|gb|BC062686.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024