NM_001079802.2(FKTN):c.559G>A (p.Gly187Ser) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jan 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000521466.4
Allele description [Variation Report for NM_001079802.2(FKTN):c.559G>A (p.Gly187Ser)]
NM_001079802.2(FKTN):c.559G>A (p.Gly187Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 30, 2024