NM_000530.8(MPZ):c.105C>A (p.Asp35Glu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004371496.1
Allele description [Variation Report for NM_000530.8(MPZ):c.105C>A (p.Asp35Glu)]
NM_000530.8(MPZ):c.105C>A (p.Asp35Glu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphor...
Sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E [Mus musculus]gi|37046741|gb|AAH57956.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024