VARIANTS

Users can search for variant data occurring on our collected genes. For each variant, we retrieved its basic annotation (gene, transcript, protein position, wildtype and mutant amino acid, codons), its association study statistics (sourced from Genebass ) and corresponding variant effect prediction scores (sourced from Ensembl ) from over 41 algorithms, including SIFT, Polyphen, PrimateAI, and AlphaMissense, normalized to facilitate comparisons. As an example, the image on the right shows violin plots summarizing effect prediction scores of 10 variants with means of these scores >= 0.7 in gene TNFSF11

Atc code example

Enter a genename, gene Ensembl ID or variant in Ensembl format

Kindly note input format for variant: Chromosome_Coordinate_Reference/Alternative allele, e.g., 20_50581449_C/G

Random variant examples

Variant ID Gene ID Gene symbol Primary transcript Details
18_6961650_C/T ENSG00000101680 LAMA1 ENST00000389658 See variant effect scores and associations
4_1248929_C/T ENSG00000159692 CTBP1 ENST00000382952 See variant effect scores and associations
4_55118622_T/C ENSG00000128052 KDR ENST00000263923 See variant effect scores and associations
12_7649551_C/T ENSG00000111701 APOBEC1 ENST00000229304 See variant effect scores and associations
9_96235471_T/A ENSG00000130948 HSD17B3 ENST00000375263 See variant effect scores and associations
1_1333711_G/T ENSG00000169962 TAS1R3 ENST00000339381 See variant effect scores and associations
2_112647352_G/T ENSG00000144136 SLC20A1 ENST00000272542 See variant effect scores and associations
1_23193265_C/A ENSG00000179546 HTR1D ENST00000374619 See variant effect scores and associations
1_17394061_G/A ENSG00000276747 PADI6 ENST00000619609 See variant effect scores and associations
11_1083546_C/T ENSG00000198788 MUC2 nan See variant effect scores and associations
20_50191178_C/T ENSG00000172216 CEBPB ENST00000303004 See variant effect scores and associations
4_182915569_G/T ENSG00000129187 DCTD ENST00000438320 See variant effect scores and associations
10_96480439_C/T ENSG00000095587 TLL2 ENST00000357947 See variant effect scores and associations
1_110673838_C/T ENSG00000177272 KCNA3 ENST00000369769 See variant effect scores and associations
3_151448125_G/A ENSG00000152580 IGSF10 ENST00000282466 See variant effect scores and associations
1_186988398_G/C ENSG00000116711 PLA2G4A ENST00000367466 See variant effect scores and associations
20_62313680_A/G ENSG00000130702 LAMA5 ENST00000252999 See variant effect scores and associations
5_56815905_C/T ENSG00000095015 MAP3K1 ENST00000399503 See variant effect scores and associations
3_101243807_G/T ENSG00000081148 IMPG2 ENST00000193391 See variant effect scores and associations
1_231421704_T/C ENSG00000135766 EGLN1 ENST00000366641 See variant effect scores and associations