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Variant : CV338898 (NM_031427.4(DNAL1):c.*7212C>G) Homo sapiens

Symbol: CV338898
Name: NM_031427.4(DNAL1):c.*7212C>G
Condition: Ciliary dyskinesia [RCV000374201]|Primary ciliary dyskinesia [RCV000374201]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: DNAL1  
Variant Type: single nucleotide variant (SO:0001624)
Source: CLINVAR
Molecular Consequence: 3 prime utr variant
Evidence: clinical testing
HGVS Name(s): NG_028083.1:g.63280C>G
NC_000014.9:g.73703154C>G
NC_000014.8:g.74169857C>G
NM_031427.3:c.*7212C>G
NM_001201366.2:c.*7212C>G
NM_031427.4:c.*7212C>G
NG_028083.2:g.63280C>G
Position
Human AssemblyChrPosition (strand)Source
GRCh381473,703,154 - 73,703,154CLINVAR
GRCh371474,169,857 - 74,169,857CLINVAR
Cytogenetic Map1414q24.3CLINVAR



Disease Annotations

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11623525
Created: 2017-01-11
Species: Homo sapiens
Last Modified: 2019-12-03
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.