NM_173354.5(SIK1):c.2048C>T (p.Pro683Leu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 28, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002318178.9
Allele description [Variation Report for NM_173354.5(SIK1):c.2048C>T (p.Pro683Leu)]
NM_173354.5(SIK1):c.2048C>T (p.Pro683Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Neuroaspergillosis
NeuroaspergillosisMedGen
-
Venezuelan equine encephalitis virus infection
Venezuelan equine encephalitis virus infectionMedGen
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Nov 10, 2024