NM_002900.3(RBP3):c.3166C>T (p.Leu1056Phe) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 4, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004443509.1
Allele description [Variation Report for NM_002900.3(RBP3):c.3166C>T (p.Leu1056Phe)]
NM_002900.3(RBP3):c.3166C>T (p.Leu1056Phe)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Endo-1,4-beta-xylanase A [Roseburia intestinalis L1-82]
Endo-1,4-beta-xylanase A [Roseburia intestinalis L1-82]gi|1583831889|emb|VCV24061.1|Protein
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See more...Assertion and evidence details
Last Updated: May 7, 2024