NM_005560.6(LAMA5):c.11068A>G (p.Ser3690Gly) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 27, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002864664.2
Allele description [Variation Report for NM_005560.6(LAMA5):c.11068A>G (p.Ser3690Gly)]
NM_005560.6(LAMA5):c.11068A>G (p.Ser3690Gly)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
SdrD B-like domain-containing protein [Agrilactobacillus fermenti]
SdrD B-like domain-containing protein [Agrilactobacillus fermenti]gi|2159756138|ref|WP_230914719.1|Protein
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Last Updated: May 1, 2024