NM_198578.4(LRRK2):c.7139C>T (p.Thr2380Ile) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 23, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004517988.1
Allele description [Variation Report for NM_198578.4(LRRK2):c.7139C>T (p.Thr2380Ile)]
NM_198578.4(LRRK2):c.7139C>T (p.Thr2380Ile)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
acetylcholine receptor subunit alpha isoform X1 [Piliocolobus tephrosceles]
acetylcholine receptor subunit alpha isoform X1 [Piliocolobus tephrosceles]gi|1297708443|ref|XP_023041767.1|Protein
-
Glyceraldehyde-3-phosphate dehydrogenase (phosphorylating) [Flagellimonas mariti...
Glyceraldehyde-3-phosphate dehydrogenase (phosphorylating) [Flagellimonas maritima]gi|1409963308|gnl|Chunlab|HME9304_0 gb|AWX45389.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 7, 2024