NM_001277115.2(DNAH11):c.12336C>T (p.Asp4112=) AND Primary ciliary dyskinesia
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000357497.6
Allele description [Variation Report for NM_001277115.2(DNAH11):c.12336C>T (p.Asp4112=)]
NM_001277115.2(DNAH11):c.12336C>T (p.Asp4112=)
Condition(s)
- Name:
- Primary ciliary dyskinesia
- Synonyms:
- Ciliary dyskinesia
- Identifiers:
- MONDO: MONDO:0016575; MedGen: C0008780; OMIM: PS244400; Human Phenotype Ontology: HP:0012265
-
DA499080 FCBBF3 Homo sapiens cDNA clone FCBBF3012656 5', mRNA sequence
DA499080 FCBBF3 Homo sapiens cDNA clone FCBBF3012656 5', mRNA sequencegi|80788158|gnl|dbEST|33244395|dbj| 080.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 16, 2024