NM_005957.5(MTHFR):c.868A>G (p.Asn290Asp) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 17, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004046079.1
Allele description [Variation Report for NM_005957.5(MTHFR):c.868A>G (p.Asn290Asp)]
NM_005957.5(MTHFR):c.868A>G (p.Asn290Asp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Ribosomal protein L19 family protein [Arabidopsis thaliana]
Ribosomal protein L19 family protein [Arabidopsis thaliana]gi|15239778|ref|NP_196736.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024