NM_003764.4(STX11):c.616G>A (p.Glu206Lys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 25, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000454862.4
Allele description [Variation Report for NM_003764.4(STX11):c.616G>A (p.Glu206Lys)]
NM_003764.4(STX11):c.616G>A (p.Glu206Lys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens
Homo sapiensRefSeq annotation of the human reference genome assemblyBioProject
-
KIF23 kinesin family member 23 [Homo sapiens]
KIF23 kinesin family member 23 [Homo sapiens]Gene ID:9493Gene
-
Gene Links for GEO Profiles (Select 5767039) (1)
Gene
-
BioProject Links for Nucleotide (Select 2217396514) (1)
BioProject
-
Gene Links for Protein (Select 530406713) (1)
Gene
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Last Updated: Dec 30, 2023