NM_015107.3(PHF8):c.2299A>G (p.Asn767Asp) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 28, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001267403.2
Allele description [Variation Report for NM_015107.3(PHF8):c.2299A>G (p.Asn767Asp)]
NM_015107.3(PHF8):c.2299A>G (p.Asn767Asp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Chain B, Crystal structure of TT0321 from Thermus thermophilus HB8
Chain B, Crystal structure of TT0321 from Thermus thermophilus HB8gi|93279186|pdb|2D1Y|BProtein
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Last Updated: Dec 24, 2023