NM_001243133.2(NLRP3):c.2172T>A (p.Thr724=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 3, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000441223.1
Allele description [Variation Report for NM_001243133.2(NLRP3):c.2172T>A (p.Thr724=)]
NM_001243133.2(NLRP3):c.2172T>A (p.Thr724=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens survivin splice variant 2 alpha mRNA, complete cds, alternatively s...
Homo sapiens survivin splice variant 2 alpha mRNA, complete cds, alternatively splicedgi|62822962|gb|AY927772.1|Nucleotide
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Last Updated: Sep 29, 2024