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Variant : CV19795 (NM_014795.4(ZEB2):c.1173_1176del (p.Thr392fs)) Homo sapiens

Symbol: CV19795
Name: NM_014795.4(ZEB2):c.1173_1176del (p.Thr392fs)
Condition: Mowat-Wilson syndrome [RCV000005022]
Clinical Significance: pathogenic
Last Evaluated: 11/26/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ZEB2  
Variant Type: deletion (SO:0001589)
Source: CLINVAR
Molecular Consequence: frameshift variant
Evidence: literature only
HGVS Name(s): NM_014795.4:c.1173_1176del
NG_016431.1:g.125378_125381del
NC_000002.12:g.144400012_144400015del
NM_001171653.2:c.1101_1104del
NC_000002.11:g.145157579_145157582del
NM_014795.3:c.1173_1176del
NP_001165124.1:p.Thr368fs
NP_055610.1:p.Thr392fs
Position
Human AssemblyChrPosition (strand)Source
GRCh382144,400,011 - 144,400,014CLINVAR
GRCh372145,157,578 - 145,157,581CLINVAR
Cytogenetic Map22q22.3CLINVAR
Age Of Onset: antenatal|neonatal/infancy



Disease Annotations
References - curated
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8558265
Created: 2014-05-13
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.