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
86651 BAA01g46070 A01 30704590 C T upstream_gene_variant MODIFIER c.-2634G>A| S146
86652 BAA01g46070 A01 30705073 C T upstream_gene_variant MODIFIER c.-3117G>A| S183
S198
86653 BAA01g46070 A01 30705309 G A upstream_gene_variant MODIFIER c.-3353C>T| S157
S163
86654 BAA01g46090 A01 30705553 G A missense_variant MODERATE c.3182C>T|p.Thr1061Ile S197
86655 BAA01g46090 A01 30706499 C T missense_variant MODERATE c.2648G>A|p.Gly883Asp S77
86656 BAA01g46080 A01 30708760 G A upstream_gene_variant MODIFIER c.-4440C>T| S119
86657 BAA01g46090 A01 30709169 C T synonymous_variant LOW c.1326G>A|p.Arg442Arg S206
S26
86658 BAA01g46090 A01 30709384 G A intron_variant MODIFIER c.1215-104C>T| S121
86659 BAA01g46090 A01 30711687 G A intron_variant MODIFIER c.786+30C>T| S272
86660 BAA01g46090 A01 30711971 C T intron_variant MODIFIER c.696+108G>A| S156
86661 BAA01g46090 A01 30712760 C T missense_variant MODERATE c.448G>A|p.Val150Ile S249
86662 BAA01g46090 A01 30713936 C T upstream_gene_variant MODIFIER c.-395G>A| S167
86663 BAA01g46090 A01 30714377 G A upstream_gene_variant MODIFIER c.-836C>T| S115
86664 BAA01g46090 A01 30714771 G A upstream_gene_variant MODIFIER c.-1230C>T| S136
86665 BAA01g46090 A01 30714837 C T upstream_gene_variant MODIFIER c.-1296G>A| S182
86666 BAA01g46090 A01 30715099 G A upstream_gene_variant MODIFIER c.-1558C>T| S274
86667 BAA01g46090 A01 30718424 C T upstream_gene_variant MODIFIER c.-4883G>A| S23
86668 BAA01g46100 A01 30720442 C T upstream_gene_variant MODIFIER c.-3112C>T| S294
86669 BAA01g46100 A01 30721582 G A upstream_gene_variant MODIFIER c.-1972G>A| S217
86670 BAA01g46100 A01 30722685 C T upstream_gene_variant MODIFIER c.-869C>T| S35
86671 BAA01g46100 A01 30725778 C T intron_variant MODIFIER c.871-25C>T| S240
86672 BAA01g46100 A01 30725977 G A intron_variant MODIFIER c.976-45G>A| S283
86673 BAA01g46100 A01 30727031 G A missense_variant MODERATE c.1565G>A|p.Cys522Tyr S241
86674 BAA01g46100 A01 30727730 G A intron_variant MODIFIER c.1708-115G>A| S296
86675 BAA01g46100 A01 30727854 C T missense_variant MODERATE c.1717C>T|p.Leu573Phe S281