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
202551 BAA02g31190 A02 18527262 G A downstream_gene_variant MODIFIER c.*4390G>A| S18
202552 BAA02g31200 A02 18529734 A T downstream_gene_variant MODIFIER c.*2018T>A| S153
S213
202553 BAA02g31200 A02 18530130 C T downstream_gene_variant MODIFIER c.*1622G>A| S123
202554 BAA02g31200 A02 18531808 C T missense_variant MODERATE c.367G>A|p.Glu123Lys S160
202555 BAA02g31200 A02 18531832 C T intron_variant MODIFIER c.356-13G>A| S9
202556 BAA02g31200 A02 18531945 C T missense_variant MODERATE c.313G>A|p.Glu105Lys S51
202557 BAA02g31200 A02 18532128 C T missense_variant MODERATE c.130G>A|p.Glu44Lys S226
202558 BAA02g31200 A02 18532882 G A upstream_gene_variant MODIFIER c.-625C>T| S72
S78
202559 BAA02g31200 A02 18532942 C T upstream_gene_variant MODIFIER c.-685G>A| S152
202560 BAA02g31200 A02 18533029 C T upstream_gene_variant MODIFIER c.-772G>A| S105
S106
202561 BAA02g31200 A02 18534488 G A upstream_gene_variant MODIFIER c.-2231C>T| S186
202562 BAA02g31200 A02 18535301 G A upstream_gene_variant MODIFIER c.-3044C>T| S156
202563 BAA02g31200 A02 18535593 G A upstream_gene_variant MODIFIER c.-3336C>T| S287
202564 BAA02g31200 A02 18535879 G A upstream_gene_variant MODIFIER c.-3622C>T| S265
202565 BAA02g31200 A02 18536023 C T upstream_gene_variant MODIFIER c.-3766G>A| S161
202566 BAA02g31200 A02 18536429 C T upstream_gene_variant MODIFIER c.-4172G>A| S231
202567 BAA02g31200 A02 18536701 G A upstream_gene_variant MODIFIER c.-4444C>T| S302
202568 BAA02g31210 A02 18539089 G A upstream_gene_variant MODIFIER c.-1080G>A| S67
202569 BAA02g31210 A02 18539279 C T upstream_gene_variant MODIFIER c.-890C>T| S140
202570 BAA02g31210 A02 18539560 C T upstream_gene_variant MODIFIER c.-609C>T| S168
S219
S278
202571 BAA02g31210 A02 18540345 G A stop_gained HIGH c.177G>A|p.Trp59* S251
202572 BAA02g31210 A02 18540866 G A intron_variant MODIFIER c.592+106G>A| S132
S137
S215
S223
S89
202573 BAA02g31210 A02 18541445 C T intron_variant MODIFIER c.593-492C>T| S52
202574 BAA02g31210 A02 18542327 G A missense_variant MODERATE c.868G>A|p.Glu290Lys S293
202575 BAA02g31210 A02 18542335 C T downstream_gene_variant MODIFIER c.*3C>T| S104
S52