NM_014639.4(SKIC3):c.4348G>T (p.Ala1450Ser) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000951215.9
Allele description [Variation Report for NM_014639.4(SKIC3):c.4348G>T (p.Ala1450Ser)]
NM_014639.4(SKIC3):c.4348G>T (p.Ala1450Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024