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CanVaS - A Greek Cancer Patient Genetic Variation Resource
ERCC2 (ERCC excision repair 2, TFIIH core complex h...)
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Curator:
Despoina Kalfakakou
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View ERCC2 gene homepage
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View all transcripts of gene ERCC2
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View all variants affecting transcripts
View unique variants in gene ERCC2
View all variants in gene ERCC2
Full data view for gene ERCC2
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View all individuals with variants in gene ERCC2
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View all diseases associated with gene ERCC2
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Legend
Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Inheritance
: Values based on OMIM's and HPO's values for inheritance.
AD
: Autosomal dominant
PI
: Autosomal dominant with paternal imprinting
MI
: Autosomal dominant with maternal imprinting
AR
: Autosomal recessive
DD
: Digenic dominant
DR
: Digenic recessive
IC
: Isolated Cases (Sporadic)
Mi
: Mitochondrial
Mu
: Multifactorial
SMo
: Somatic mosaicism
SMu
: Somatic mutation
OG
: Oligogenic (3 genes)
PG
: Polygenic (>3 genes)
XL
: X-linked
XLD
: X-linked dominant
XLR
: X-linked recessive
YL
: Y-linked
3 entries on 1 page. Showing entries 1 - 3.
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ID
Abbreviation
Name
OMIM ID
Inheritance
Individuals
Phenotypes
Associated with genes
Associated tissues
Disease features
00001
BrCa
Breast Cancer
114480
-
4048
4505
ATM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, NTHL1, PALB2, RAD51C, RAD51D, TP53
breast
-
00104
FANCN
Fanconi anemia, complementation group N
610832
-
0
0
PALB2
-
-
00105
PNCA3
Pancreatic cancer, susceptibility to, 3
613348
-
0
0
PALB2
pancreas
-
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