NM_002473.6(MYH9):c.2296G>A (p.Gly766Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004040215.1
Allele description [Variation Report for NM_002473.6(MYH9):c.2296G>A (p.Gly766Ser)]
NM_002473.6(MYH9):c.2296G>A (p.Gly766Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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url- eggc.vipKAv (445)
BioProject
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Serratia plymuthica strain VR42 16S ribosomal RNA gene, partial sequence
Serratia plymuthica strain VR42 16S ribosomal RNA gene, partial sequencegi|955285628|gb|KT228271.1|Nucleotide
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"Centre for Mendelian Genomics, University Medical Centre Ljublja... (2)
"Centre for Mendelian Genomics, University Medical Centre Ljubljana"[submitter] AND "MYO6"[gene]SearchClinVar
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See more...Assertion and evidence details
Last Updated: May 7, 2024