NM_000527.5(LDLR):c.1164C>T (p.His388=) AND Hypercholesterolemia, familial, 1
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 5, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004010555.2
Allele description [Variation Report for NM_000527.5(LDLR):c.1164C>T (p.His388=)]
NM_000527.5(LDLR):c.1164C>T (p.His388=)
Condition(s)
- Name:
- Hypercholesterolemia, familial, 1
- Synonyms:
- LDL RECEPTOR DISORDER; Hyperlipoproteinemia Type IIa; HYPER-LOW-DENSITY-LIPOPROTEINEMIA; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0007750; MedGen: C0745103; Orphanet: 391665; OMIM: 143890
-
Homo sapiens leptin receptor overlapping transcript (LEPROT), transcript variant...
Homo sapiens leptin receptor overlapping transcript (LEPROT), transcript variant 1, mRNAgi|1519245339|ref|NM_017526.5|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024