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variants: 3265166

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
3265166 2:64843299:A:ACG rs201820436 2 64843299 A ACG 0.0620223 0.0325068 0.0437927 0.0527479 0.0020362 0.0285375 0.0731707 0.0847365 0.0357321 Intronic       ncRNA_intronic ENSG00000287123       0.018 0.116 -30176.654296875 -30228.681640625 -52.02734375 -30285.3271484375 -30333.259765625 -47.9326171875 -31074.4820300775 -31125.6118103058 -51.1297802282461 -15261.8876953125 -13848.3120117188 1413.57568359375 -17504.5302734375 -15140.5676269531 2363.96264648438 -17402.4552132023 -15323.5407825872 2078.91443061508 Q1_0-20% AF_0-0.2     0
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