NM_198578.4(LRRK2):c.6538T>A (p.Ser2180Thr) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 10, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004517951.1
Allele description [Variation Report for NM_198578.4(LRRK2):c.6538T>A (p.Ser2180Thr)]
NM_198578.4(LRRK2):c.6538T>A (p.Ser2180Thr)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
cytochrome oxidase subunit 1, partial (mitochondrion) [Cionus hortulanus]
cytochrome oxidase subunit 1, partial (mitochondrion) [Cionus hortulanus]gi|1169307582|gb|ARB57184.1|Protein
-
cytochrome c oxidase subunit 1, partial (mitochondrion) [Cionus hortulanus]
cytochrome c oxidase subunit 1, partial (mitochondrion) [Cionus hortulanus]gi|1837664191|gb|QJP23477.1|Protein
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See more...Assertion and evidence details
Last Updated: May 7, 2024