NM_001044385.3(TMEM237):c.1159+166A>G AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001586358.3
Allele description [Variation Report for NM_001044385.3(TMEM237):c.1159+166A>G]
NM_001044385.3(TMEM237):c.1159+166A>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
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Last Updated: Dec 24, 2023