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Variant : CV663072 (NM_000722.4(CACNA2D1):c.1038+276T>G) Homo sapiens

Symbol: CV663072
Name: NM_000722.4(CACNA2D1):c.1038+276T>G
Condition: not provided [RCV000843437]
Clinical Significance: benign
Last Evaluated: 06/14/2018
Review Status: criteria provided, single submitter
Related Genes: CACNA2D1  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: clinical testing
HGVS Name(s): NM_000722.4:c.1038+276T>G
NM_001366867.1:c.1038+276T>G
NG_009358.2:g.410915T>G
NC_000007.14:g.82037801A>C
NC_000007.13:g.81667117A>C
NM_000722.2:c.1038+276T>G
Position
Human AssemblyChrPosition (strand)Source
GRCh38782,037,801 - 82,037,801CLINVAR
GRCh37781,667,117 - 81,667,117CLINVAR
Cytogenetic Map77q21.11CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14745498
Created: 2019-09-06
Species: Homo sapiens
Last Modified: 2019-11-05
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.