rs730881832
|
Entrez Id: |
4595 |
Gene Symbol: |
MUTYH |
MUTYH
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs730881832
|
Entrez Id: |
4595 |
Gene Symbol: |
MUTYH |
MUTYH
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation |
CLINVAR |
RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.
|
25525159 |
2015 |
rs730881832
|
Entrez Id: |
4595 |
Gene Symbol: |
MUTYH |
MUTYH
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation |
CLINVAR |
Functional Complementation Assay for 47 MUTYH Variants in a MutY-Disrupted Escherichia coli Strain.
|
25820570 |
2015 |
rs730881832
|
Entrez Id: |
4595 |
Gene Symbol: |
MUTYH |
MUTYH
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation |
CLINVAR |
Analysis of MUTYH genotypes and colorectal phenotypes in patients With MUTYH-associated polyposis.
|
19032956 |
2009 |
rs730881832
|
Entrez Id: |
4595 |
Gene Symbol: |
MUTYH |
MUTYH
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation |
CLINVAR |
Increased colorectal cancer incidence in obligate carriers of heterozygous mutations in MUTYH.
|
19394335 |
2009 |
rs730881832
|
Entrez Id: |
4595 |
Gene Symbol: |
MUTYH |
MUTYH
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation |
CLINVAR |
Expanded extracolonic tumor spectrum in MUTYH-associated polyposis.
|
19732775 |
2009 |
rs730881832
|
Entrez Id: |
4595 |
Gene Symbol: |
MUTYH |
MUTYH
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation |
CLINVAR |
Base-excision repair of oxidative DNA damage.
|
17581577 |
2007 |
rs730881832
|
Entrez Id: |
4595 |
Gene Symbol: |
MUTYH |
MUTYH
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation |
CLINVAR |
Colorectal cancer and inherited mutations in base-excision repair.
|
15465463 |
2004 |
rs730881832
|
Entrez Id: |
4595 |
Gene Symbol: |
MUTYH |
MUTYH
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation |
CLINVAR |
Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH.
|
12853198 |
2003 |