NM_012216.4(MID2):c.1090G>T (p.Ala364Ser) AND Intellectual disability, X-linked 101
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003225874.8
Allele description [Variation Report for NM_012216.4(MID2):c.1090G>T (p.Ala364Ser)]
NM_012216.4(MID2):c.1090G>T (p.Ala364Ser)
Condition(s)
Assertion and evidence details
Last Updated: Nov 24, 2024