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Variant : CV26187 (NM_000390.4(CHM):c.1358_1359delinsGA (p.Ser453Ter)) Homo sapiens

Symbol: CV26187
Name: NM_000390.4(CHM):c.1358_1359delinsGA (p.Ser453Ter)
Condition: Choroideremia [RCV000011898]
Clinical Significance: pathogenic
Last Evaluated: 11/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CHM  
Variant Type: indel (SO:0001587)
Source: CLINVAR
Molecular Consequence: stop-gain|nonsense
Evidence: literature only
HGVS Name(s): NM_001362518.2:c.914_915delinsGA
NM_001362519.1:c.914_915delinsGA
LRG_699:g.151862_151863delinsGA
NG_009874.2:g.151862_151863delinsGA
NC_000023.11:g.85900700_85900701delinsTC
NM_000390.4:c.1358_1359delinsGA
NM_001320959.1:c.914_915delinsGA
NM_001362517.1:c.914_915delinsGA
NC_000023.10:g.85155705_85155706delinsTC
NP_001307888.1:p.Ser305Ter
NP_001349446.1:p.Ser305Ter
NP_001349447.1:p.Ser305Ter
NP_001349448.1:p.Ser305Ter
NP_000381.1:p.Ser453Ter
LRG_699t1:c.1358_1359delCCinsGA
LRG_699p1:p.Ser453Ter
Position
Human AssemblyChrPosition (strand)Source
GRCh38X85,900,700 - 85,900,701CLINVAR
GRCh37X85,155,705 - 85,155,706CLINVAR
Cytogenetic MapXXq21.2CLINVAR
Age Of Onset: adolescence / young adulthood|adolescent|childhood
Prevalence: 1-9 / 100 000



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8562209
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2019-09-10
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.