NM_002016.2(FLG):c.10430G>A (p.Arg3477His) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 3, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004386716.1
Allele description [Variation Report for NM_002016.2(FLG):c.10430G>A (p.Arg3477His)]
NM_002016.2(FLG):c.10430G>A (p.Arg3477His)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
LPXTG-anchored aggregation substance [Enterococcus faecalis]
LPXTG-anchored aggregation substance [Enterococcus faecalis]gi|2721255890|ref|WP_342080506.1|Protein
-
LPD1 domain-containing protein [Enterococcus faecalis]
LPD1 domain-containing protein [Enterococcus faecalis]gi|2721255887|ref|WP_342080503.1|Protein
-
Mus musculus SLAM family member 6 (Slamf6), transcript variant 2, mRNA
Mus musculus SLAM family member 6 (Slamf6), transcript variant 2, mRNAgi|1102835202|ref|NM_001347186.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024