NM_006941.4(SOX10):c.927T>C (p.His309=) AND Waardenburg syndrome type 4C
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 15, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001808575.10
Allele description [Variation Report for NM_006941.4(SOX10):c.927T>C (p.His309=)]
NM_006941.4(SOX10):c.927T>C (p.His309=)
Condition(s)
-
Homo sapiens chromosome 11, GRCh38.p14 Primary Assembly
Homo sapiens chromosome 11, GRCh38.p14 Primary Assemblygi|568815587|gnl|ASM:GCF_000001305| f|NC_000011.10||gpp|GPC_000001303.1||gnl|NCBI_GENOMES|11Nucleotide
-
Mus musculus
Mus musculusTranscriptional and epigenetic profiling of aged mouse SVZ-derived neural stem / progenitor cellsBioProject
-
BioProject Links for BioSample (Select 7407200) (1)
BioProject
-
Conserved Domain Links for Protein (Select 225698433) (1)
Conserved Domains
-
GEO DataSets Links for BioSample (Select 14853710) (1)
GEO DataSets
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See more...Assertion and evidence details
Last Updated: May 12, 2024