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Variant : CV631594 (NM_015896.4(ZMYND10):c.674A>G (p.His225Arg)) Homo sapiens

Symbol: CV631594
Name: NM_015896.4(ZMYND10):c.674A>G (p.His225Arg)
Condition: Primary ciliary dyskinesia [RCV000823199]
Clinical Significance: uncertain significance
Last Evaluated: 10/18/2018
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+174A>G
NM_015896.4:c.674A>G
NG_023270.1:g.2993A>G
NG_042828.1:g.7803A>G
NC_000003.12:g.50342944T>C
NC_000003.11:g.50380375T>C
NM_015896.2:c.674A>G
NP_056980.2:p.His225Arg
Position
Human AssemblyChrPosition (strand)Source
GRCh38350,342,944 - 50,342,944CLINVAR
GRCh37350,380,375 - 50,380,375CLINVAR
Cytogenetic Map33p21.31CLINVAR
Trait Synonyms: Immotile cilia syndrome; Polynesian bronchiectasis



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14743086
Created: 2019-09-06
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.