NM_006623.4(PHGDH):c.498C>T (p.Ser166=) AND PHGDH deficiency
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 13, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002890009.3
Allele description [Variation Report for NM_006623.4(PHGDH):c.498C>T (p.Ser166=)]
NM_006623.4(PHGDH):c.498C>T (p.Ser166=)
Condition(s)
-
Synthetic construct Mus musculus clone IMAGE:100064120, MGC:193491 a disintegrin...
Synthetic construct Mus musculus clone IMAGE:100064120, MGC:193491 a disintegrin and metallopeptidase domain 22 (Adam22) mRNA, encodes complete proteingi|182888080|gb|BC160376.1|Nucleotide
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Last Updated: Sep 29, 2024