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Variant : CV267362 (NM_014780.4(CUL7):c.594G>A (p.Gln198=)) Homo sapiens

Symbol: CV267362
Name: NM_014780.4(CUL7):c.594G>A (p.Gln198=)
Condition: not specified [RCV000395014]
Clinical Significance: uncertain significance
Last Evaluated: 09/28/2015
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.594G>A
NG_016205.1:g.7196G>A
NC_000006.12:g.43051750C>T
NC_000006.11:g.43019488C>T
NP_055595.2:p.Gln198=
Position
Human AssemblyChrPosition (strand)Source
GRCh38643,051,750 - 43,051,750CLINVAR
GRCh37643,019,488 - 43,019,488CLINVAR
Cytogenetic Map66p21.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11643487
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.