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variants: 2496746

One row per variant. Variant_ID = Chromosome:Position:Ref:Alt (GRCh38). Allele frequencies are gnomAD v4.1 joint (joint + 8 ancestries). Free-text search box covers rsID, gene symbol and amino-acid change.

Data license: Apache License 2.0

This data as json

rowid Variant_ID RSID Chromosome Position Reference_Allele Alternate_Allele Joint_AF African_AF Admixed_American_AF Ashkenazi_Jewish_AF East_Asian_AF Finnish_AF Middle_Eastern_AF Non_Finnish_European_AF South_Asian_AF ENCODE_cCRE_Annotation Repeat_Name Repeat_Class Repeat_Family Functional_Annotation Gene Gene_Detail Exonic_Function Amino_Acid_Change PhastCons_100way PhyloP_100way Evo2_7B_NoRC_Ref Evo2_7B_NoRC_Alt Evo2_7B_NoRC_Delta Evo2_7B_AvgRC_Ref Evo2_7B_AvgRC_Alt Evo2_7B_AvgRC_Delta Evo2_7B_WeightedRC_Ref Evo2_7B_WeightedRC_Alt Evo2_7B_WeightedRC_Delta Evo2_40B_NoRC_Ref Evo2_40B_NoRC_Alt Evo2_40B_NoRC_Delta Evo2_40B_AvgRC_Ref Evo2_40B_AvgRC_Alt Evo2_40B_AvgRC_Delta Evo2_40B_WeightedRC_Ref Evo2_40B_WeightedRC_Alt Evo2_40B_WeightedRC_Delta MAF_tier AF_bin SCREEN_V4_Classes SCREEN_V4_Accessions SCREEN_V4_Overlap_Count
2496746 18:24906458:C:G rs77703883 18 24906458 C G 0.905883 0.970202 0.915589 0.823631 0.968352 0.870451 0.846939 0.879039 0.776786 Intronic L1PA5 LINE L1 ncRNA_intronic ENSG00000266573       0.007 -0.2995 -30635.8828125 -30642.44140625 -6.55859375 -30913.220703125 -30924.1552734375 -10.9345703125 -27740.2387463263 -27745.82429496 -5.58554863369136 -15266.220703125 -15278.833984375 -12.61328125 -18189.4111328125 -16021.7978515625 2167.61328125 -15820.5324048743 -14775.2570689642 1045.27533591014 Q2_20-40% AF_0.8-1.0     0
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