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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g45980 A06 29261581 C T upstream_gene_variant MODIFIER c.-826C>T| S17
2 BAA06g45980 A06 29264095 C T missense_variant MODERATE c.848C>T|p.Pro283Leu S202
3 BAA06g45980 A06 29264198 C T intron_variant MODIFIER c.892-31C>T| S252
4 BAA06g45980 A06 29264202 G A intron_variant MODIFIER c.892-27G>A| S284
5 BAA06g45980 A06 29264718 C T intron_variant MODIFIER c.984+397C>T| S242
6 BAA06g45980 A06 29267414 A T intron_variant MODIFIER c.1088-1721A>T| S302
7 BAA06g45980 A06 29269499 G A intron_variant MODIFIER c.1152+300G>A| S152
8 BAA06g45980 A06 29270218 C T intron_variant MODIFIER c.1226-53C>T| S302
9 BAA06g45980 A06 29273546 C T downstream_gene_variant MODIFIER c.*46C>T| S264
10 BAA06g45980 A06 29274253 G A downstream_gene_variant MODIFIER c.*753G>A| S12
11 BAA06g45980 A06 29275476 C T downstream_gene_variant MODIFIER c.*1976C>T| S132
S215
S89
12 BAA06g45980 A06 29275978 G A downstream_gene_variant MODIFIER c.*2478G>A| S199
13 BAA06g45980 A06 29277138 C T downstream_gene_variant MODIFIER c.*3638C>T| S279
14 BAA06g45980 A06 29277204 C T downstream_gene_variant MODIFIER c.*3704C>T| S155
S211
15 BAA06g45980 A06 29277495 C T downstream_gene_variant MODIFIER c.*3995C>T| S259
16 BAA06g45980 A06 29278065 G A downstream_gene_variant MODIFIER c.*4565G>A| S35