NM_080628.3(TLDC2):c.182T>C (p.Ile61Thr) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 29, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002788067.1
Allele description
NM_080628.3(TLDC2):c.182T>C (p.Ile61Thr)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
PREDICTED: Homo sapiens nucleoredoxin like 2 (NXNL2), transcript variant X2, mRN...
PREDICTED: Homo sapiens nucleoredoxin like 2 (NXNL2), transcript variant X2, mRNAgi|2462497436|ref|XM_054333084.1|Nucleotide
-
Homo sapiens IQ motif containing K (IQCK), transcript variant 6, mRNA
Homo sapiens IQ motif containing K (IQCK), transcript variant 6, mRNAgi|2033622736|ref|NM_001394804.1|Nucleotide
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Last Updated: Feb 13, 2023