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Variant : CV328759 (NM_139319.3(SLC17A8):c.*1295T>C) Homo sapiens

Symbol: CV328759
Name: NM_139319.3(SLC17A8):c.*1295T>C
Condition: Nonsyndromic Hearing Loss, Dominant [RCV000318288]
Clinical Significance: likely benign
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.69376T>C
NC_000012.12:g.100421454T>C
NC_000012.11:g.100815232T>C
NM_001145288.2:c.*1295T>C
NM_139319.3:c.*1295T>C
NM_139319.2:c.*1295T>C
Position
Human AssemblyChrPosition (strand)Source
GRCh3812100,421,454 - 100,421,454CLINVAR
GRCh3712100,815,232 - 100,815,232CLINVAR
Cytogenetic Map1212q23.1CLINVAR



Disease Annotations

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 11618845
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.