NM_005629.4(SLC6A8):c.30C>T (p.Ile10=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 7, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000441339.8
Allele description [Variation Report for NM_005629.4(SLC6A8):c.30C>T (p.Ile10=)]
NM_005629.4(SLC6A8):c.30C>T (p.Ile10=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 26, 2024