NM_000890.5(KCNJ5):c.1151C>T (p.Pro384Leu) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 5, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001767120.2
Allele description [Variation Report for NM_000890.5(KCNJ5):c.1151C>T (p.Pro384Leu)]
NM_000890.5(KCNJ5):c.1151C>T (p.Pro384Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
VWA7 von Willebrand factor A domain containing 7 [Homo sapiens]
VWA7 von Willebrand factor A domain containing 7 [Homo sapiens]Gene ID:80737Gene
-
Gene Links for GEO Profiles (Select 132506685) (1)
Gene
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Last Updated: Dec 24, 2023