NM_002055.5(GFAP):c.488T>C (p.Leu163Pro) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 1, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000996565.17
Allele description [Variation Report for NM_002055.5(GFAP):c.488T>C (p.Leu163Pro)]
NM_002055.5(GFAP):c.488T>C (p.Leu163Pro)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 12, 2024