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Variant : CV315669 (NM_139319.3(SLC17A8):c.913A>G (p.Thr305Ala)) Homo sapiens

Symbol: CV315669
Name: NM_139319.3(SLC17A8):c.913A>G (p.Thr305Ala)
Condition: Nonsyndromic Hearing Loss, Dominant [RCV000338898]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: SLC17A8  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: clinical testing
HGVS Name(s): NG_021175.1:g.50527A>G
NC_000012.12:g.100402605A>G
NC_000012.11:g.100796383A>G
NP_647480.1:p.Thr305Ala
NM_001145288.2:c.903+126A>G
NM_139319.3:c.913A>G
NM_139319.2:c.913A>G
Position
Human AssemblyChrPosition (strand)Source
GRCh3812100,402,605 - 100,402,605CLINVAR
GRCh3712100,796,383 - 100,796,383CLINVAR
Cytogenetic Map1212q23.1CLINVAR



Disease Annotations

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 11607087
Created: 2017-01-11
Species: Homo sapiens
Last Modified: 2019-11-12
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.