NM_001031709.3(RNLS):c.691C>T (p.Arg231Cys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 29, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002901850.1
Allele description
NM_001031709.3(RNLS):c.691C>T (p.Arg231Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
hypothetical protein BOSOLAPHORUS_179 [Erwinia phage vB_EamM_Bosolaphorus]
hypothetical protein BOSOLAPHORUS_179 [Erwinia phage vB_EamM_Bosolaphorus]gi|1315517126|gb|AUG85966.1|Protein
-
DA919224 SMINT2 Homo sapiens cDNA clone SMINT2004341 5', mRNA sequence
DA919224 SMINT2 Homo sapiens cDNA clone SMINT2004341 5', mRNA sequencegi|82069166|gnl|dbEST|33698676|dbj| 224.1|Nucleotide
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Chain A, EXFOLIATIVE TOXIN B
Chain A, EXFOLIATIVE TOXIN Bgi|6137706|pdb|1QTF|AProtein
-
Branchiootic syndrome 3
Branchiootic syndrome 3MedGen
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See more...Assertion and evidence details
Last Updated: Feb 13, 2023