rs121907900
|
|
|
0.710 |
GeneticVariation |
BEFREE |
WT1 gene mutations have been described in 46,XY patients with ambiguous genitalia or complete gonadal dysgenesis with or without Wilms' tumor, nephropathy, gonadoblastoma, and other defects, e.g., cryptorchidism or hypospadias. p.R462W is a hot spot mutation in exon 9 and is the most common mutation in patients with Denys-Drash syndrome.
|
29320783 |
2017 |
rs1564969626
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit.
|
27241786 |
2016 |
rs28941778
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1414739809
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Genetic analysis revealed a de novo heterozygous missense mutation c.1186G>A (p.Asp396Asn) in the WT1 gene, confirming the diagnosis of DDS.
|
24379226 |
2014 |
rs760336723
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The Wt1+/R394W mouse displays glomerulosclerosis and early-onset renal failure characteristic of human Denys-Drash syndrome.
|
15509792 |
2004 |
rs772590420
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We examined three DDS associated mutations in ZF2 of human WT1 where the normal glutamine at position 369 is replaced by arginine (Q369R), lysine (Q369K) or histidine (Q369H).
|
27596598 |
2016 |
rs121907900
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
|
|
|
rs1060501253
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121907901
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121907902
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121907903
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121907904
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121907905
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121907906
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121907907
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121907909
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Exon 9 mutations in the WT1 gene, without influencing KTS splice isoforms, are also responsible for Frasier syndrome.
|
10571943 |
1999 |
rs121907909
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Genetic screening in adolescents with steroid-resistant nephrotic syndrome.
|
23515051 |
2013 |
rs121907909
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology.
|
9108089 |
1997 |
rs121907909
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children.
|
21851196 |
2011 |
rs1423753702
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology.
|
9108089 |
1997 |
rs1554939839
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Twenty-four new cases of WT1 germline mutations and review of the literature: genotype/phenotype correlations for Wilms tumor development.
|
15150775 |
2004 |
rs1554945232
|
|
TC |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1554946500
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1554946600
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1565000973
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|