NM_005236.3(ERCC4):c.2423C>G (p.Ala808Gly) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003353046.2
Allele description [Variation Report for NM_005236.3(ERCC4):c.2423C>G (p.Ala808Gly)]
NM_005236.3(ERCC4):c.2423C>G (p.Ala808Gly)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Attractin-like 1 [synthetic construct]
Attractin-like 1 [synthetic construct]gi|195934785|gb|AAI68382.1|Protein
-
604231 (1)
OMIM
-
124097 (1)
OMIM
-
ACT domain repeat 3 [Arabidopsis thaliana]
ACT domain repeat 3 [Arabidopsis thaliana]gi|18411317|ref|NP_565146.1|Protein
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Last Updated: Sep 29, 2024