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variants: 2505767

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
2505767 18:28750073:A:G rs356929 18 28750073 A G 0.704212 0.666844 0.622036 0.801038 0.485008 0.783674 0.780822 0.7403 0.726631 Intronic L1P1 LINE L1 ncRNA_intronic ENSG00000265994       0.009 -0.5765 -28232.17578125 -28237.1484375 -4.97265625 -28263.8022460938 -28270.9189453125 -7.11669921875 -28301.0521010017 -28309.2261443222 -8.17404332049045 -14878.7734375 -13073.5390625 1805.234375 -15648.6118164062 -13375.5258789062 2273.0859375 -15505.9466156418 -13427.6786852899 2078.26793035189 Q3_40-60% AF_0.6-0.8     0
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