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Variant : CV943632 (NM_015896.4(ZMYND10):c.601C>T (p.Leu201Phe)) Homo sapiens

Symbol: CV943632
Name: NM_015896.4(ZMYND10):c.601C>T (p.Leu201Phe)
Condition: Primary ciliary dyskinesia [RCV001237984]
Clinical Significance: uncertain significance
Last Evaluated: 11/12/2019
Review Status: criteria provided, single submitter
Related Genes: ZMYND10  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: clinical testing
HGVS Name(s): NM_001308379.2:c.599+101C>T
NM_015896.4:c.601C>T
NG_023270.1:g.2920C>T
NG_042828.1:g.7730C>T
NC_000003.12:g.50343017G>A
NC_000003.11:g.50380448G>A
NM_015896.2:c.601C>T
NP_056980.2:p.Leu201Phe
Position
Human AssemblyChrPosition (strand)Source
GRCh38350,343,017 - 50,343,017CLINVAR
GRCh37350,380,448 - 50,380,448CLINVAR
Cytogenetic Map33p21.31CLINVAR
Trait Synonyms: Immotile cilia syndrome; Polynesian bronchiectasis



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 38488537
Created: 2020-08-11
Species: Homo sapiens
Last Modified: 2020-10-15
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.