NM_005993.5(TBCD):c.2366G>C (p.Gly789Ala) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 28, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002717718.2
Allele description [Variation Report for NM_005993.5(TBCD):c.2366G>C (p.Gly789Ala)]
NM_005993.5(TBCD):c.2366G>C (p.Gly789Ala)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens chemokine-like factor super family member 8 (CKLFSF8) mRNA, complet...
Homo sapiens chemokine-like factor super family member 8 (CKLFSF8) mRNA, complete cdsgi|25167350|gb|AF474370.2|Nucleotide
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Last Updated: May 1, 2024