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Variant : CV502517 (NM_000722.4(CACNA2D1):c.1086G>A (p.Thr362=)) Homo sapiens

Symbol: CV502517
Name: NM_000722.4(CACNA2D1):c.1086G>A (p.Thr362=)
Condition: not specified [RCV000610155]
Clinical Significance: likely benign
Last Evaluated: 02/14/2017
Review Status: criteria provided, single submitter
Related Genes: CACNA2D1  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: clinical testing
HGVS Name(s): LRG_437:g.415862G>A
NG_009358.2:g.415862G>A
NC_000007.14:g.82032854C>T
NC_000007.13:g.81662170C>T
NM_000722.2:c.1086G>A
NP_000713.2:p.Thr362=
LRG_437t1:c.1086G>A
NM_000722.4:c.1086G>A
NM_001366867.1:c.1086G>A
NP_001353796.1:p.Thr362=
Position
Human AssemblyChrPosition (strand)Source
GRCh38782,032,854 - 82,032,854CLINVAR
GRCh37781,662,170 - 81,662,170CLINVAR
Cytogenetic Map77q21.11CLINVAR
Trait Synonyms: AllHighlyPenetrant




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13537255
Created: 2018-05-08
Species: Homo sapiens
Last Modified: 2019-11-12
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.