Advanced search

Combine gene, variant, phenotype, region and year filters

Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.

Transparent by designEvery result links extracted entities to its source sentence and publication identifier.

Publications

1 records shown · first 60
TypeEntitySource evidenceConfidenceExtractor
variantrs1326605“A synonymous variant p. (Asp395Asp), rs1896976 and two intronic SNPs viz., rs1326605, and rs1571084 were found in all tumors tested.”0.90hgvs_regex_v1
genePKHD1“Identification of PKHD1 mutations in Brain, Breast and Rectal tumors by Next Generation DNA Sequencing.”0.98hgnc_dict_v1
phenotypepolycystic kidney disease“INTRODUCTION: It is well established that the PKHD1 mutations are associated with autosomal recessive polycystic kidney disease (ARPKD).”0.98phenotype_alias_lexicon_v2
variantrs113562492“In phyllodes tumor of breast, two unique missense variants were detected (rs113562492) p. (Met2841Val); and (rs137972270) in p. (Arg589Cys) and these variants are not present in other tumors tested.”0.90hgvs_regex_v1