NM_003737.4(DCHS1):c.4708C>T (p.Arg1570Trp) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002545469.2
Allele description [Variation Report for NM_003737.4(DCHS1):c.4708C>T (p.Arg1570Trp)]
NM_003737.4(DCHS1):c.4708C>T (p.Arg1570Trp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
microtubule-associated protein tau, isoform CRA_h [Mus musculus]
microtubule-associated protein tau, isoform CRA_h [Mus musculus]gi|148702270|gb|EDL34217.1||gnl|WGS |mCP93986Protein
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baseplate assembly protein [Nostoc phage A1]
baseplate assembly protein [Nostoc phage A1]gi|1026924899|gb|AND75601.1|Protein
-
beta-galactoside alpha-2,6-sialyltransferase, partial [Rattus norvegicus]
beta-galactoside alpha-2,6-sialyltransferase, partial [Rattus norvegicus]gi|554420|gb|AAB06269.1|Protein
-
Appendix Cancer - StatPearls
Appendix Cancer - StatPearls
-
SAOUHSC_02647 [Staphylococcus aureus subsp. aureus NCTC 8325]
SAOUHSC_02647 [Staphylococcus aureus subsp. aureus NCTC 8325]Gene ID:3921209Gene
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Last Updated: May 1, 2024