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Variant : CV166028 (NM_024330.4(SLC27A3):c.1447+19G>A) Homo sapiens

Symbol: CV166028
Name: NM_024330.4(SLC27A3):c.1447+19G>A
Condition: not provided [RCV000162289]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: SLC27A3  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: literature only
HGVS Name(s): NC_000001.11:g.153778572G>A
NC_000001.10:g.153751048G>A
NG_053029.1:g.8281G>A
NM_024330.1:c.1588+19G>A
NM_001317929.4:c.1447+19G>A
NM_024330.4:c.1447+19G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh381153,778,572 - 153,778,572CLINVAR
GRCh371153,751,048 - 153,751,048CLINVAR
Cytogenetic Map11q21.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9850479
Created: 2015-04-07
Species: Homo sapiens
Last Modified: 2020-01-07
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.