|
rs587779852
|
|
T |
0.720 |
CausalMutation |
CLINVAR |
MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing.
|
24451234 |
2014 |
|
rs587779852
|
|
T |
0.720 |
CausalMutation |
CLINVAR |
Ten new ATM alterations in Polish patients with ataxia-telangiectasia.
|
25614872 |
2014 |
|
rs587779852
|
|
|
0.720 |
GeneticVariation |
BEFREE |
We now report that a nonsense mutation, p.E1978X (c.5932G>T), is both a classical A-T mutation and a breast cancer susceptibility allele in Eastern European populations.
|
18807267 |
2009 |
|
rs587779852
|
|
T |
0.720 |
CausalMutation |
CLINVAR |
We now report that a nonsense mutation, p.E1978X (c.5932G>T), is both a classical A-T mutation and a breast cancer susceptibility allele in Eastern European populations.
|
18807267 |
2009 |
|
rs587779852
|
|
T |
0.720 |
CausalMutation |
CLINVAR |
Founder effects for ATM gene mutations in Italian Ataxia Telangiectasia families.
|
19691550 |
2009 |
|
rs587779852
|
|
T |
0.720 |
CausalMutation |
CLINVAR |
Contribution of mutations in ATM to breast cancer development in the Czech population.
|
18497957 |
2008 |
|
rs587779852
|
|
T |
0.720 |
CausalMutation |
CLINVAR |
DHPLC screening of ATM gene in Italian patients affected by ataxia-telangiectasia: fourteen novel ATM mutations.
|
17124347 |
2006 |
|
rs587779852
|
|
|
0.720 |
GeneticVariation |
BEFREE |
The Mennonite mutation, 5932 G>T, is common in Russian A-T families, and the STR haplovariants are the same in both Poland and Russia.
|
16266405 |
2005 |
|
rs587779852
|
|
T |
0.720 |
CausalMutation |
CLINVAR |
ATM mutations, haplotype analysis, and immunological status of Russian patients with ataxia telangiectasia.
|
15880721 |
2005 |
|
rs587779852
|
|
T |
0.720 |
CausalMutation |
CLINVAR |
The Mennonite mutation, 5932 G>T, is common in Russian A-T families, and the STR haplovariants are the same in both Poland and Russia.
|
16266405 |
2005 |
|
rs587779852
|
|
T |
0.720 |
CausalMutation |
CLINVAR |
Splicing defects in the ataxia-telangiectasia gene, ATM: underlying mutations and consequences.
|
10330348 |
1999 |