NM_022489.4(INF2):c.34G>A (p.Ala12Thr) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 23, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001235906.7
Allele description [Variation Report for NM_022489.4(INF2):c.34G>A (p.Ala12Thr)]
NM_022489.4(INF2):c.34G>A (p.Ala12Thr)
Condition(s)
Assertion and evidence details
Last Updated: Sep 1, 2024