NM_001144060.2(NHSL1):c.2360C>T (p.Thr787Met) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 27, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004207142.1
Allele description [Variation Report for NM_001144060.2(NHSL1):c.2360C>T (p.Thr787Met)]
NM_001144060.2(NHSL1):c.2360C>T (p.Thr787Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Model organism or animal sample from Grammomys cometes
Model organism or animal sample from Grammomys cometesbiosample
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Last Updated: Aug 18, 2024