NM_002241.5(KCNJ10):c.1137C>G (p.Val379=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 15, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002314146.9
Allele description [Variation Report for NM_002241.5(KCNJ10):c.1137C>G (p.Val379=)]
NM_002241.5(KCNJ10):c.1137C>G (p.Val379=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
carcinoembryonic antigen [Homo sapiens]
carcinoembryonic antigen [Homo sapiens]gi|180227|gb|AAA51969.1|Protein
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024