NM_198578.4(LRRK2):c.7109G>T (p.Ser2370Ile) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004517986.1
Allele description [Variation Report for NM_198578.4(LRRK2):c.7109G>T (p.Ser2370Ile)]
NM_198578.4(LRRK2):c.7109G>T (p.Ser2370Ile)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
MFS transporter, MCP family, solute carrier family 16 (monocarboxylic acid trans...
MFS transporter, MCP family, solute carrier family 16 (monocarboxylic acid transporters), member 10 [Exophiala dermatitidis NIH/UT8656]gi|684170444|ref|XP_009159093.1|Protein
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See more...Assertion and evidence details
Last Updated: May 7, 2024