NM_198578.4(LRRK2):c.4275G>T (p.Gln1425His) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003182584.2
Allele description [Variation Report for NM_198578.4(LRRK2):c.4275G>T (p.Gln1425His)]
NM_198578.4(LRRK2):c.4275G>T (p.Gln1425His)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
PREDICTED: Homo sapiens calcium voltage-gated channel auxiliary subunit alpha2de...
PREDICTED: Homo sapiens calcium voltage-gated channel auxiliary subunit alpha2delta 1 (CACNA2D1), transcript variant X1, mRNAgi|1370510936|ref|XM_006716118.3|Nucleotide
-
106422[uid] AND (alive[prop]) (0)
Gene
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Last Updated: May 1, 2024