NM_198578.4(LRRK2):c.3334C>T (p.Leu1112Phe) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002326515.2
Allele description [Variation Report for NM_198578.4(LRRK2):c.3334C>T (p.Leu1112Phe)]
NM_198578.4(LRRK2):c.3334C>T (p.Leu1112Phe)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
JGI_CAAP13976.rev NIH_XGC_tropInt1 Xenopus tropicalis cDNA clone IMAGE:7720575 3...
JGI_CAAP13976.rev NIH_XGC_tropInt1 Xenopus tropicalis cDNA clone IMAGE:7720575 3', mRNA sequencegi|58797744|gnl|dbEST|27691136|gb|C 27.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024