NM_006494.4(ERF):c.1088C>T (p.Ser363Leu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002882846.2
Allele description [Variation Report for NM_006494.4(ERF):c.1088C>T (p.Ser363Leu)]
NM_006494.4(ERF):c.1088C>T (p.Ser363Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
histone H3, partial [Chartergellus zonatus]
histone H3, partial [Chartergellus zonatus]gi|2277201649|gb|UTY77845.1|Protein
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Last Updated: May 1, 2024