Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
172851 BAA02g16500 A02 8071272 G A missense_variant MODERATE c.512G>A|p.Arg171Lys S174
S27
172852 BAA02g16510 A02 8072447 C T upstream_gene_variant MODIFIER c.-2356C>T| S181
172853 BAA02g16510 A02 8073144 G A upstream_gene_variant MODIFIER c.-1659G>A| S161
172854 BAA02g16510 A02 8073622 T A upstream_gene_variant MODIFIER c.-1181T>A| S265
172855 BAA02g16510 A02 8074284 G A upstream_gene_variant MODIFIER c.-519G>A| S193
172856 BAA02g16510 A02 8075030 C T synonymous_variant LOW c.228C>T|p.Ile76Ile S201
172857 BAA02g16510 A02 8075041 C T missense_variant MODERATE c.239C>T|p.Ala80Val S249
172858 BAA02g16500 A02 8075628 C T downstream_gene_variant MODIFIER c.*4235C>T| S212
172859 BAA02g16510 A02 8078675 G A downstream_gene_variant MODIFIER c.*3168G>A| S74
172860 BAA02g16520 A02 8079492 C T missense_variant MODERATE c.473G>A|p.Ser158Asn S167
172861 BAA02g16510 A02 8080010 C T downstream_gene_variant MODIFIER c.*4503C>T| S15
S3
172862 BAA02g16520 A02 8080220 C T missense_variant MODERATE c.127G>A|p.Glu43Lys S135
172863 BAA02g16520 A02 8080253 G A missense_variant MODERATE c.94C>T|p.Leu32Phe S247
172864 BAA02g16520 A02 8080778 C T upstream_gene_variant MODIFIER c.-432G>A| S44
172865 BAA02g16520 A02 8083236 G A upstream_gene_variant MODIFIER c.-2890C>T| S169
172866 BAA02g16520 A02 8083491 G A upstream_gene_variant MODIFIER c.-3145C>T| S12
172867 BAA02g16520 A02 8084406 G A upstream_gene_variant MODIFIER c.-4060C>T| S231
172868 BAA02g16520 A02 8084647 C T upstream_gene_variant MODIFIER c.-4301G>A| S282
172869 BAA02g16530 A02 8084675 G A missense_variant MODERATE c.1667C>T|p.Pro556Leu S80
172870 BAA02g16530 A02 8085187 C T synonymous_variant LOW c.1155G>A|p.Glu385Glu S54
172871 BAA02g16530 A02 8085196 G C synonymous_variant LOW c.1146C>G|p.Thr382Thr S54
172872 BAA02g16530 A02 8085210 C T missense_variant MODERATE c.1132G>A|p.Val378Ile S219
S72
172873 BAA02g16540 A02 8085758 G A downstream_gene_variant MODIFIER c.*3264C>T| S172
S217
172874 BAA02g16530 A02 8086553 G A missense_variant MODERATE c.47C>T|p.Pro16Leu S52
172875 BAA02g16530 A02 8088740 C T upstream_gene_variant MODIFIER c.-2141G>A| S117