NM_001256715.2(DNAAF3):c.1062G>C (p.Pro354=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003425435.8
Allele description
NM_001256715.2(DNAAF3):c.1062G>C (p.Pro354=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
LOC127271099 [Homo sapiens]
LOC127271099 [Homo sapiens]Gene ID:127271099Gene
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See more...Assertion and evidence details
Last Updated: Aug 4, 2024