NM_001134438.2(PHLDB2):c.112C>G (p.Leu38Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004291795.1
Allele description [Variation Report for NM_001134438.2(PHLDB2):c.112C>G (p.Leu38Val)]
NM_001134438.2(PHLDB2):c.112C>G (p.Leu38Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
THNSL1 threonine synthase like 1 [Homo sapiens]
THNSL1 threonine synthase like 1 [Homo sapiens]Gene ID:79896Gene
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See more...Assertion and evidence details
Last Updated: Jun 2, 2024