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
74651 BAA01g39340 A01 26124155 C T intron_variant MODIFIER c.262+3185G>A| S89
74652 BAA01g39340 A01 26124198 C T intron_variant MODIFIER c.262+3142G>A| S39
74653 BAA01g39340 A01 26124316 G A intron_variant MODIFIER c.262+3024C>T| S122
74654 BAA01g39340 A01 26124818 G A intron_variant MODIFIER c.262+2522C>T| S152
74655 BAA01g39340 A01 26124876 C T intron_variant MODIFIER c.262+2464G>A| S256
74656 BAA01g39340 A01 26125335 G A intron_variant MODIFIER c.262+2005C>T| S2
74657 BAA01g39340 A01 26126309 C T intron_variant MODIFIER c.262+1031G>A| S18
74658 BAA01g39350 A01 26126611 G A upstream_gene_variant MODIFIER c.-4798G>A| S229
74659 BAA01g39340 A01 26130334 C T upstream_gene_variant MODIFIER c.-2733G>A| S77
S82
74660 BAA01g39350 A01 26131589 G A missense_variant MODERATE c.181G>A|p.Glu61Lys S38
74661 BAA01g39340 A01 26132180 G A upstream_gene_variant MODIFIER c.-4579C>T| S224
74662 BAA01g39340 A01 26132441 G A upstream_gene_variant MODIFIER c.-4840C>T| S117
74663 BAA01g39350 A01 26134312 C T downstream_gene_variant MODIFIER c.*136C>T| S240
74664 BAA01g39350 A01 26134414 G A downstream_gene_variant MODIFIER c.*238G>A| S252
74665 BAA01g39350 A01 26134755 C T downstream_gene_variant MODIFIER c.*579C>T| S274
74666 BAA01g39350 A01 26135252 G A downstream_gene_variant MODIFIER c.*1076G>A| S117
74667 BAA01g39350 A01 26135918 G A downstream_gene_variant MODIFIER c.*1742G>A| S173
74668 BAA01g39350 A01 26136427 C T downstream_gene_variant MODIFIER c.*2251C>T| S94
74669 BAA01g39350 A01 26136512 C T downstream_gene_variant MODIFIER c.*2336C>T| S79
S84
74670 BAA01g39350 A01 26137346 T C downstream_gene_variant MODIFIER c.*3170T>C| S99
74671 BAA01g39350 A01 26137971 C T downstream_gene_variant MODIFIER c.*3795C>T| S242
74672 BAA01g39360 A01 26138082 C T missense_variant MODERATE c.469G>A|p.Asp157Asn S233
74673 BAA01g39360 A01 26138279 G A missense_variant MODERATE c.376C>T|p.Leu126Phe S229
74674 BAA01g39360 A01 26138660 C T upstream_gene_variant MODIFIER c.-6G>A| S107
74675 BAA01g39360 A01 26140010 G A upstream_gene_variant MODIFIER c.-1356C>T| S297