NM_001122630.2(CDKN1C):c.567_578del (p.186_187AP[8]) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002519777.2
Allele description [Variation Report for NM_001122630.2(CDKN1C):c.567_578del (p.186_187AP[8])]
NM_001122630.2(CDKN1C):c.567_578del (p.186_187AP[8])
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
MAG: inorganic pyrophosphatase [Chloroflexi bacterium 54-19]
MAG: inorganic pyrophosphatase [Chloroflexi bacterium 54-19]gi|1113331168|gb|OJV95172.1||gnl|WG J|BGO39_24475Protein
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024