NM_020754.4(ARHGAP31):c.820C>T (p.Pro274Ser) AND not provided
- Germline classification:
- Benign/Likely benign (5 submissions)
- Last evaluated:
- Jun 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000428753.18
Allele description [Variation Report for NM_020754.4(ARHGAP31):c.820C>T (p.Pro274Ser)]
NM_020754.4(ARHGAP31):c.820C>T (p.Pro274Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024