NM_007254.4(PNKP):c.1397T>C (p.Met466Thr) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 16, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002318595.9
Allele description [Variation Report for NM_007254.4(PNKP):c.1397T>C (p.Met466Thr)]
NM_007254.4(PNKP):c.1397T>C (p.Met466Thr)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
BEL1-like homeodomain protein 2 [Cucurbita maxima]
BEL1-like homeodomain protein 2 [Cucurbita maxima]gi|1280988326|ref|XP_022977654.1|Protein
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Last Updated: Sep 29, 2024