NM_002253.4(KDR):c.3888T>A (p.Ser1296=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 10, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000869240.3
Allele description [Variation Report for NM_002253.4(KDR):c.3888T>A (p.Ser1296=)]
NM_002253.4(KDR):c.3888T>A (p.Ser1296=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024