rs147105770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Deep phenotyping of 89 xeroderma pigmentosum patients reveals unexpected heterogeneity dependent on the precise molecular defect.
|
26884178 |
2016 |
rs147105770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Physical interaction between SLX4 (FANCP) and XPF (FANCQ) proteins and biological consequences of interaction-defective missense mutations.
|
26453996 |
2015 |
rs147105770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
The ERCC1 and ERCC4 (XPF) genes and gene products.
|
26074087 |
2015 |
rs147105770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia.
|
23623389 |
2013 |
rs1555468482
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia.
|
23623389 |
2013 |
rs397509403
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia.
|
23623389 |
2013 |
rs121913049
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Physiological consequences of defects in ERCC1-XPF DNA repair endonuclease.
|
21612988 |
2011 |
rs147105770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Physiological consequences of defects in ERCC1-XPF DNA repair endonuclease.
|
21612988 |
2011 |
rs121913049
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mislocalization of XPF-ERCC1 nuclease contributes to reduced DNA repair in XP-F patients.
|
20221251 |
2010 |
rs147105770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Mislocalization of XPF-ERCC1 nuclease contributes to reduced DNA repair in XP-F patients.
|
20221251 |
2010 |
rs764731249
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy.
|
10447254 |
1999 |
rs769679311
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy.
|
10447254 |
1999 |
rs121913049
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease.
|
9579555 |
1998 |
rs764731249
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Characterization of molecular defects in xeroderma pigmentosum group F in relation to its clinically mild symptoms.
|
9580660 |
1998 |
rs764731249
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease.
|
9579555 |
1998 |
rs769679311
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease.
|
9579555 |
1998 |
rs769679311
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Characterization of molecular defects in xeroderma pigmentosum group F in relation to its clinically mild symptoms.
|
9580660 |
1998 |
rs121913049
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease.
|
8797827 |
1996 |
rs764731249
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease.
|
8797827 |
1996 |
rs769679311
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease.
|
8797827 |
1996 |
rs147105770
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs869025184
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs912480692
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs2276466
|
|
|
0.040 |
GeneticVariation |
BEFREE |
Impact of XPF rs2276466 polymorphism on cancer susceptibility: a meta-analysis.
|
31040199 |
2019 |
rs2276466
|
|
|
0.040 |
GeneticVariation |
BEFREE |
We investigated the association between polymorphisms in excision repair cross-complementation group 1 (ERCC1) (rs3212986, rs2298881 and rs11615) and xeroderma pigmentosum-complementation group F (XPF) (rs2276466 and rs6498486) and risk of colorectal cancer.
|
24861646 |
2014 |