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Variant : CV322563 (NM_139319.3(SLC17A8):c.*1306C>T) Homo sapiens

Symbol: CV322563
Name: NM_139319.3(SLC17A8):c.*1306C>T
Condition: Nonsyndromic Hearing Loss, Dominant [RCV000377612]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: SLC17A8  
Variant Type: single nucleotide variant (SO:0001624)
Source: CLINVAR
Molecular Consequence: 3 prime utr variant
Evidence: clinical testing
HGVS Name(s): NG_021175.1:g.69387C>T
NC_000012.12:g.100421465C>T
NC_000012.11:g.100815243C>T
NM_001145288.2:c.*1306C>T
NM_139319.3:c.*1306C>T
NM_139319.2:c.*1306C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh3812100,421,465 - 100,421,465CLINVAR
GRCh3712100,815,243 - 100,815,243CLINVAR
Cytogenetic Map1212q23.1CLINVAR



Disease Annotations

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 11661545
Created: 2017-01-11
Species: Homo sapiens
Last Modified: 2019-12-03
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.