NM_018344.6(SLC29A3):c.874G>C (p.Asp292His) AND H syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001244325.7
Allele description [Variation Report for NM_018344.6(SLC29A3):c.874G>C (p.Asp292His)]
NM_018344.6(SLC29A3):c.874G>C (p.Asp292His)
Condition(s)
- Name:
- H syndrome
- Synonyms:
- Histiocytosis with joint contractures and sensorineural deafness; Faisalabad histiocytosis; HISTIOCYTOSIS AND LYMPHADENOPATHY WITH OR WITHOUT CUTANEOUS, CARDIAC, AND/OR ENDOCRINE FEATURES, JOINT CONTRACTURES, AND/OR DEAFNESS; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0011273; MedGen: C1864445; Orphanet: 168569; OMIM: 602782
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Mus musculus fission, mitochondrial 1 (Fis1), transcript variant 1, mRNA; nuclea...
Mus musculus fission, mitochondrial 1 (Fis1), transcript variant 1, mRNA; nuclear gene for mitochondrial productgi|253735729|ref|NM_025562.3|Nucleotide
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"16065-90-0"[CompleteSynonym] (1)
PubChem Compound
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See more...Assertion and evidence details
Last Updated: Feb 20, 2024