NM_198578.4(LRRK2):c.5004G>T (p.Leu1668=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002343082.2
Allele description [Variation Report for NM_198578.4(LRRK2):c.5004G>T (p.Leu1668=)]
NM_198578.4(LRRK2):c.5004G>T (p.Leu1668=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Chain H, Carboxylesterase
Chain H, Carboxylesterasegi|2694303196|pdb|8ILT|HProtein
-
PREDICTED: expansin-B3 [Populus euphratica]
PREDICTED: expansin-B3 [Populus euphratica]gi|743892744|ref|XP_011039743.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024