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Variant : CV662501 (NM_000722.4(CACNA2D1):c.295-41C>T) Homo sapiens

Symbol: CV662501
Name: NM_000722.4(CACNA2D1):c.295-41C>T
Condition: not provided [RCV000834090]
Clinical Significance: likely benign
Last Evaluated: 06/16/2018
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.295-41C>T
NM_001302890.2:c.295-41C>T
NM_001366867.1:c.295-41C>T
NG_009358.2:g.278066C>T
NC_000007.14:g.82170650G>A
NC_000007.13:g.81799966G>A
NM_000722.2:c.295-41C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh38782,170,650 - 82,170,650CLINVAR
GRCh37781,799,966 - 81,799,966CLINVAR
Cytogenetic Map77q21.11CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14726938
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.