NM_003824.4(FADD):c.286+12G>C AND FADD-related immunodeficiency
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 8, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003639351.2
Allele description [Variation Report for NM_003824.4(FADD):c.286+12G>C]
NM_003824.4(FADD):c.286+12G>C
Condition(s)
-
Homo sapiens complement receptor 1 (KN) gene, KN*01.E29+2G_T allele, exon 29 and...
Homo sapiens complement receptor 1 (KN) gene, KN*01.E29+2G_T allele, exon 29 and partial cdsgi|2367707146|gb|OM201363.1|Nucleotide
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Last Updated: Sep 29, 2024