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Variant : CV374064 (NM_001013703.4(EIF2AK4):c.4562-8G>T) Homo sapiens

Symbol: CV374064
Name: NM_001013703.4(EIF2AK4):c.4562-8G>T
Condition: Pulmonary venoocclusive disease 2, autosomal recessive [RCV000999788]|not specified [RCV000427404]
Clinical Significance: benign
Last Evaluated: 08/24/2018
Review Status: criteria provided, multiple submitters, no conflicts|criteria provided, single submitter
Related Genes: EIF2AK4  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: clinical testing
HGVS Name(s): NG_034053.1:g.101228G>T
NC_000015.10:g.40030351G>T
NC_000015.9:g.40322552G>T
NM_001013703.4:c.4562-8G>T
NM_001013703.2:c.4562-8G>T
NM_001013703.3:c.4562-8G>T
Position
Human AssemblyChrPosition (strand)Source
GRCh381540,030,351 - 40,030,351CLINVAR
GRCh371540,322,552 - 40,322,552CLINVAR
Cytogenetic Map1515q15.1CLINVAR
Trait Synonyms: AllHighlyPenetrant; Familial pulmonary capillary hemangiomatosis; Pulmonary venoocclusive disease 2



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12838685
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-11-24
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.