NM_001190764.2(TMEM238):c.238T>C (p.Phe80Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004274000.1
Allele description [Variation Report for NM_001190764.2(TMEM238):c.238T>C (p.Phe80Leu)]
NM_001190764.2(TMEM238):c.238T>C (p.Phe80Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
ante -7 eggcsite.comr8H (0)
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Last Updated: Jun 2, 2024