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Variant : CV563108 (NM_015896.4(ZMYND10):c.830C>T (p.Ala277Val)) Homo sapiens

Symbol: CV563108
Name: NM_015896.4(ZMYND10):c.830C>T (p.Ala277Val)
Condition: Primary ciliary dyskinesia [RCV000684918]
Clinical Significance: uncertain significance
Last Evaluated: 03/01/2018
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_023270.1:g.3497C>T
NG_042828.1:g.8307C>T
NM_015896.2:c.830C>T
NC_000003.11:g.50379871G>A
NC_000003.12:g.50342440G>A
NP_056980.2:p.Ala277Val
NM_001308379.2:c.815C>T
NM_015896.4:c.830C>T
NP_001295308.1:p.Ala272Val
Position
Human AssemblyChrPosition (strand)Source
GRCh38350,342,440 - 50,342,440CLINVAR
GRCh37350,379,871 - 50,379,871CLINVAR
Cytogenetic Map33p21.31CLINVAR
Trait Synonyms: Immotile cilia syndrome; Polynesian bronchiectasis



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13803460
Created: 2018-11-06
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.