NM_001379500.1(COL18A1):c.107-12197G>A AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 10, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002527466.2
Allele description [Variation Report for NM_001379500.1(COL18A1):c.107-12197G>A]
NM_001379500.1(COL18A1):c.107-12197G>A
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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eggcsite.comzIj (0)
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PopSet Links for Nucleotide (Select 1194992446) (1)
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Bos taurus D-loop, partial sequence; mitochondrial.
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Last Updated: May 19, 2024