NM_001605.3(AARS1):c.700C>T (p.Pro234Ser) AND not provided
- Germline classification:
- Likely benign (3 submissions)
- Last evaluated:
- Mar 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000488107.28
Allele description [Variation Report for NM_001605.3(AARS1):c.700C>T (p.Pro234Ser)]
NM_001605.3(AARS1):c.700C>T (p.Pro234Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 4, 2024