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Variant : CV267419 (NM_014780.4(CUL7):c.3273G>A (p.Ser1091=)) Homo sapiens

Symbol: CV267419
Name: NM_014780.4(CUL7):c.3273G>A (p.Ser1091=)
Condition: not specified [RCV000335036]
Clinical Significance: uncertain significance
Last Evaluated: 09/08/2015
Review Status: criteria provided, single submitter
Related Genes: CUL7  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: clinical testing
HGVS Name(s): NM_014780.4:c.3273G>A
NG_016205.1:g.15416G>A
NC_000006.12:g.43043530C>T
NC_000006.11:g.43011268C>T
NP_055595.2:p.Ser1091=
Position
Human AssemblyChrPosition (strand)Source
GRCh38643,043,530 - 43,043,530CLINVAR
GRCh37643,011,268 - 43,011,268CLINVAR
Cytogenetic Map66p21.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11640316
Created: 2017-01-11
Species: Homo sapiens
Last Modified: 2019-08-06
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.