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Variant : CV658240 (NM_014795.4(ZEB2):c.593-240C>A) Homo sapiens

Symbol: CV658240
Name: NM_014795.4(ZEB2):c.593-240C>A
Condition: not provided [RCV000834823]
Clinical Significance: likely benign
Last Evaluated: 06/19/2018
Review Status: criteria provided, single submitter
Related Genes: ZEB2  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: clinical testing
HGVS Name(s): NM_001171653.2:c.521-240C>A
NM_014795.4:c.593-240C>A
NG_016431.1:g.121022C>A
NC_000002.12:g.144404370G>T
NC_000002.11:g.145161937G>T
NM_014795.3:c.593-240C>A
Position
Human AssemblyChrPosition (strand)Source
GRCh382144,404,370 - 144,404,370CLINVAR
GRCh372145,161,937 - 145,161,937CLINVAR
Cytogenetic Map22q22.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14728547
Created: 2019-09-06
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.