NM_004431.5(EPHA2):c.1892T>C (p.Met631Thr) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 31, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000828286.3
Allele description [Variation Report for NM_004431.5(EPHA2):c.1892T>C (p.Met631Thr)]
NM_004431.5(EPHA2):c.1892T>C (p.Met631Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024