NM_000522.5(HOXA13):c.538C>T (p.Pro180Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002859238.2
Allele description [Variation Report for NM_000522.5(HOXA13):c.538C>T (p.Pro180Ser)]
NM_000522.5(HOXA13):c.538C>T (p.Pro180Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Prunella rubeculoides transforming growth factor beta-2 (TGFB2) gene, partial cd...
Prunella rubeculoides transforming growth factor beta-2 (TGFB2) gene, partial cdsgi|1818983920|gb|MT051532.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024