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
176701 BAA02g18530 A02 9442105 C A missense_variant MODERATE c.1474C>A|p.Leu492Met S252
176702 BAA02g18530 A02 9442107 G A synonymous_variant LOW c.1476G>A|p.Leu492Leu S122
176703 BAA02g18530 A02 9442304 C T missense_variant MODERATE c.1673C>T|p.Ala558Val S124
176704 BAA02g18530 A02 9442909 C T missense_variant MODERATE c.2215C>T|p.Leu739Phe S6
176705 BAA02g18530 A02 9444166 G A downstream_gene_variant MODIFIER c.*1249G>A| S132
S137
S215
176706 BAA02g18530 A02 9444774 G A downstream_gene_variant MODIFIER c.*1857G>A| S202
176707 BAA02g18530 A02 9445657 C T downstream_gene_variant MODIFIER c.*2740C>T| S9
176708 BAA02g18530 A02 9445792 G A downstream_gene_variant MODIFIER c.*2875G>A| S43
176709 BAA02g18530 A02 9446911 G A downstream_gene_variant MODIFIER c.*3994G>A| S297
176710 BAA02g18540 A02 9449865 G A upstream_gene_variant MODIFIER c.-2437G>A| S193
176711 BAA02g18540 A02 9449889 C T upstream_gene_variant MODIFIER c.-2413C>T| S301
S304
176712 BAA02g18540 A02 9451158 C T upstream_gene_variant MODIFIER c.-1144C>T| S182
176713 BAA02g18540 A02 9451881 C T upstream_gene_variant MODIFIER c.-421C>T| S93
176714 BAA02g18540 A02 9452108 C T upstream_gene_variant MODIFIER c.-194C>T| S266
176715 BAA02g18540 A02 9452556 C T synonymous_variant LOW c.255C>T|p.Asp85Asp S189
S226
S250
S41
176716 BAA02g18540 A02 9452760 T A missense_variant MODERATE c.459T>A|p.Asp153Glu S216
176717 BAA02g18540 A02 9454019 C T intron_variant MODIFIER c.754+964C>T| S293
176718 BAA02g18540 A02 9455271 G A intron_variant MODIFIER c.754+2216G>A| S157
S166
176719 BAA02g18540 A02 9456449 C T intron_variant MODIFIER c.754+3394C>T| S100
176720 BAA02g18540 A02 9456561 C T intron_variant MODIFIER c.755-3331C>T| S84
S93
176721 BAA02g18540 A02 9457803 C T intron_variant MODIFIER c.755-2089C>T| S277
176722 BAA02g18540 A02 9457857 G A intron_variant MODIFIER c.755-2035G>A| S193
176723 BAA02g18540 A02 9458238 G A intron_variant MODIFIER c.755-1654G>A| S86
176724 BAA02g18540 A02 9459891 G A splice_acceptor_variant&intron_variant HIGH c.755-1G>A| S232
176725 BAA02g18540 A02 9460240 C T missense_variant MODERATE c.1103C>T|p.Ala368Val S2