NM_000505.4(F12):c.952G>C (p.Ala318Pro) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004385792.1
Allele description [Variation Report for NM_000505.4(F12):c.952G>C (p.Ala318Pro)]
NM_000505.4(F12):c.952G>C (p.Ala318Pro)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
cytochrome b, partial (mitochondrion) [Chiromyscus chiropus]
cytochrome b, partial (mitochondrion) [Chiromyscus chiropus]gi|1852459694|gb|QKO28448.1|Protein
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See more...Assertion and evidence details
Last Updated: May 7, 2024