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Variant : CV636351 (NM_000722.4(CACNA2D1):c.2760G>C (p.Trp920Cys)) Homo sapiens

Symbol: CV636351
Name: NM_000722.4(CACNA2D1):c.2760G>C (p.Trp920Cys)
Condition: Brugada syndrome [RCV000809634]
Clinical Significance: uncertain significance
Last Evaluated: 11/30/2018
Review Status: criteria provided, single submitter
Related Genes: CACNA2D1  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: clinical testing
HGVS Name(s): NM_000722.4:c.2760G>C
NM_001366867.1:c.2796G>C
LRG_437:g.484640G>C
NG_009358.2:g.484640G>C
NC_000007.14:g.81964076C>G
NC_000007.13:g.81593392C>G
NM_000722.3:c.2760G>C
NP_000713.2:p.Trp920Cys
NP_001353796.1:p.Trp932Cys
Position
Human AssemblyChrPosition (strand)Source
GRCh38781,964,076 - 81,964,076CLINVAR
GRCh37781,593,392 - 81,593,392CLINVAR
Cytogenetic Map77q21.11CLINVAR
Trait Synonyms: Sudden Unexplained Death Syndrome; Sudden unexplained nocturnal death syndrome; Sudden Unexplained Nocturnal Death Syndrome (SUNDS)



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14710543
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.