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Variant : CV239242 (NM_015896.4(ZMYND10):c.1105C>T (p.Arg369Trp)) Homo sapiens

Symbol: CV239242
Name: NM_015896.4(ZMYND10):c.1105C>T (p.Arg369Trp)
Condition: Primary ciliary dyskinesia [RCV000233474]
Clinical Significance: benign
Last Evaluated: 02/27/2019
Review Status: criteria provided, single submitter
Related Genes: ZMYND10  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: clinical testing
HGVS Name(s): NG_042828.1:g.8921C>T
NC_000003.12:g.50341826G>A
NC_000003.11:g.50379257G>A
NM_015896.2:c.1105C>T
NP_056980.2:p.Arg369Trp
O75800:p.Arg369Trp
NM_001308379.2:c.1090C>T
NM_015896.4:c.1105C>T
NG_023270.1:g.4111C>T
NP_001295308.1:p.Arg364Trp
Position
Human AssemblyChrPosition (strand)Source
GRCh38350,341,826 - 50,341,826CLINVAR
GRCh37350,379,257 - 50,379,257CLINVAR
Cytogenetic Map33p21.31CLINVAR
Trait Synonyms: Immotile cilia syndrome; Polynesian bronchiectasis



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11350157
Created: 2016-07-12
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.