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Variant : CV315365 (NM_032273.4(TMEM126A):c.-16G>C) Homo sapiens

Symbol: CV315365
Name: NM_032273.4(TMEM126A):c.-16G>C
Condition: Optic Atrophy, Recessive [RCV000282094]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: TMEM126A  
Variant Type: single nucleotide variant (SO:0001623)
Source: CLINVAR
Molecular Consequence: 5 prime utr variant
Evidence: clinical testing
HGVS Name(s): NG_017157.1:g.5163G>C
NC_000011.10:g.85648081G>C
NC_000011.9:g.85359125G>C
NM_001244735.1:c.-133G>C
NM_032273.4:c.-16G>C
NG_017157.2:g.5163G>C
NM_032273.3:c.-16G>C
Position
Human AssemblyChrPosition (strand)Source
GRCh381185,648,081 - 85,648,081CLINVAR
GRCh371185,359,125 - 85,359,125CLINVAR
Cytogenetic Map1111q14.1CLINVAR



Disease Annotations

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 11601479
Created: 2017-01-11
Species: Homo sapiens
Last Modified: 2020-03-17
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.