NM_003227.4(TFR2):c.523C>G (p.Leu175Val) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003375715.2
Allele description [Variation Report for NM_003227.4(TFR2):c.523C>G (p.Leu175Val)]
NM_003227.4(TFR2):c.523C>G (p.Leu175Val)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
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