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Variant : CV608841 (Single allele) Homo sapiens

Symbol: CV608841
Name: Single allele
Condition: Renal transitional cell carcinoma [RCV000754611]
Clinical Significance: likely pathogenic
Last Evaluated: 01/14/2019
Review Status: no assertion criteria provided
Related Genes: ADCK2   AGBL3   AKR1B1   AKR1B10   AKR1B15   AKR1D1   ATP6V0A4   BPGM   BRAF   CALD1   CEP41   CHCHD3   CHRM2   CLEC2L   CNOT4   COPG2   CPA1   CPA2   CPA4   CPA5   CREB3L2   CYREN   DENND2A   DGKI   EXOC4   FAM180A   FMC1   FMC1-LUC7L2   KDM7A   KIAA1549   KLF14   KLHDC10   KLRG2   LRGUK   LUC7L2   LUZP6   MEST   MESTIT1   MIR182   MIR183   MIR29A   MIR29B1   MIR335   MIR96   MKLN1   MKRN1   MTPN   NDUFB2   NRF1   NUP205   PARP12   PLXNA4   PODXL   PTN   RAB19   SLC13A4   SLC35B4   SLC37A3   SSMEM1   STMP1   STRA8   SVOPL   TBXAS1   TMEM140   TMEM209   TMEM213   TRIM24   TSGA13   TTC26   UBE2H   UBN2   WDR91   ZC3HAV1   ZC3HAV1L   ZC3HC1  
Variant Type: complex (SO:0001784)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh377129,367,205 - 140,482,957CLINVAR
Cytogenetic Map77q32.2-34CLINVAR
Trait Synonyms: renal TCC; Renal urothelial carcinoma




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14352097
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-14
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.