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Variant : CV655139 (NM_014795.4(ZEB2):c.2627A>G (p.Asp876Gly)) Homo sapiens

Symbol: CV655139
Name: NM_014795.4(ZEB2):c.2627A>G (p.Asp876Gly)
Condition: not provided [RCV000841938]
Clinical Significance: likely benign
Last Evaluated: 04/17/2018
Review Status: criteria provided, single submitter
Related Genes: ZEB2  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: clinical testing
HGVS Name(s): NM_001171653.2:c.2555A>G
NM_014795.4:c.2627A>G
NG_016431.1:g.126832A>G
NC_000002.12:g.144398560T>C
NC_000002.11:g.145156127T>C
NM_014795.3:c.2627A>G
NP_001165124.1:p.Asp852Gly
NP_055610.1:p.Asp876Gly
Position
Human AssemblyChrPosition (strand)Source
GRCh382144,398,560 - 144,398,560CLINVAR
GRCh372145,156,127 - 145,156,127CLINVAR
Cytogenetic Map22q22.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14743270
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.