NM_003824.4(FADD):c.6C>T (p.Asp2=) AND FADD-related immunodeficiency
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 26, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001479154.7
Allele description [Variation Report for NM_003824.4(FADD):c.6C>T (p.Asp2=)]
NM_003824.4(FADD):c.6C>T (p.Asp2=)
Condition(s)
-
SAMN37277413 (1)
SRA
-
Homo sapiens fibronectin 1 (FN1), transcript variant 9, mRNA
Homo sapiens fibronectin 1 (FN1), transcript variant 9, mRNAgi|1831772094|ref|NM_001306130.2|Nucleotide
-
unnamed protein product [Homo sapiens]
unnamed protein product [Homo sapiens]gi|189053861|dbj|BAG36124.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024