NM_018124.4(RFWD3):c.1294C>T (p.His432Tyr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003728111.1
Allele description [Variation Report for NM_018124.4(RFWD3):c.1294C>T (p.His432Tyr)]
NM_018124.4(RFWD3):c.1294C>T (p.His432Tyr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024