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Variant : CV658132 (NM_014795.4(ZEB2):c.917-275T>C) Homo sapiens

Symbol: CV658132
Name: NM_014795.4(ZEB2):c.917-275T>C
Condition: not provided [RCV000827834]
Clinical Significance: 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.845-275T>C
NM_014795.4:c.917-275T>C
NG_016431.1:g.124847T>C
NC_000002.12:g.144400545A>G
NC_000002.11:g.145158112A>G
NM_014795.3:c.917-275T>C
Position
Human AssemblyChrPosition (strand)Source
GRCh382144,400,545 - 144,400,545CLINVAR
GRCh372145,158,112 - 145,158,112CLINVAR
Cytogenetic Map22q22.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14710834
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.