NM_002016.2(FLG):c.2630A>G (p.Gln877Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002944977.2
Allele description [Variation Report for NM_002016.2(FLG):c.2630A>G (p.Gln877Arg)]
NM_002016.2(FLG):c.2630A>G (p.Gln877Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
transmembrane 4 L6 family member 20 isoform 1 [Mus musculus]
transmembrane 4 L6 family member 20 isoform 1 [Mus musculus]gi|13384858|ref|NP_079729.1|Protein
-
eIF4A [Solenopsis invicta]
eIF4A [Solenopsis invicta]Gene ID:105208077Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024