NM_024884.3(L2HGDH):c.137C>T (p.Thr46Ile) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 10, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000501806.7
Allele description [Variation Report for NM_024884.3(L2HGDH):c.137C>T (p.Thr46Ile)]
NM_024884.3(L2HGDH):c.137C>T (p.Thr46Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: May 26, 2024