NM_000233.4(LHCGR):c.866+63G>C AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 26, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001696568.1
Allele description [Variation Report for NM_000233.4(LHCGR):c.866+63G>C]
NM_000233.4(LHCGR):c.866+63G>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Retinal Cone Dystrophy 1 [Supplementary Concept]
Retinal Cone Dystrophy 1 [Supplementary Concept]aka RCD1<br/>Date introduced: November 5, 2012<br/>MeSH
-
elastin isoform X16 [Homo sapiens]
elastin isoform X16 [Homo sapiens]gi|2217365863|ref|XP_047275914.1|Protein
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Last Updated: Sep 1, 2024