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Variant : CV550297 (NM_024706.5(ZNF668):c.1009A>G (p.Lys337Glu)) Homo sapiens

Symbol: CV550297
Name: NM_024706.5(ZNF668):c.1009A>G (p.Lys337Glu)
Condition: not provided [RCV000677298]
Clinical Significance: uncertain significance
Last Evaluated: 06/21/2018
Review Status: criteria provided, single submitter
Related Genes: ZNF668  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: clinical testing
HGVS Name(s): NM_001172670.1:c.1009A>G
NM_001172669.1:c.1078A>G
NP_001166141.1:p.Lys337Glu
NC_000016.10:g.31061919T>C
NC_000016.9:g.31073240T>C
NM_001172668.1:c.1009A>G
NP_001166139.1:p.Lys337Glu
NP_078982.3:p.Lys337Glu
NP_001166140.1:p.Lys360Glu
NM_024706.5:c.1009A>G
Position
Human AssemblyChrPosition (strand)Source
GRCh381631,061,919 - 31,061,919CLINVAR
GRCh371631,073,240 - 31,073,240 (+)CLINVAR
Cytogenetic Map1616p11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13790417
Created: 2018-09-11
Species: Homo sapiens
Last Modified: 2020-01-07
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.