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


Gene ID

Results: 1 - 26 of 26 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g17630 A08 14342958 C T upstream_gene_variant MODIFIER c.-3614C>T| S32
2 BAA08g17630 A08 14343035 G A upstream_gene_variant MODIFIER c.-3537G>A| S298
3 BAA08g17630 A08 14343441 G A upstream_gene_variant MODIFIER c.-3131G>A| S108
4 BAA08g17630 A08 14343709 C T upstream_gene_variant MODIFIER c.-2863C>T| S277
5 BAA08g17630 A08 14343918 G A upstream_gene_variant MODIFIER c.-2654G>A| S238
6 BAA08g17630 A08 14344842 C T upstream_gene_variant MODIFIER c.-1730C>T| S233
7 BAA08g17630 A08 14345740 C T upstream_gene_variant MODIFIER c.-832C>T| S251
8 BAA08g17630 A08 14345843 G A upstream_gene_variant MODIFIER c.-729G>A| S64
9 BAA08g17630 A08 14346617 C T missense_variant MODERATE c.46C>T|p.Pro16Ser S178
10 BAA08g17630 A08 14347810 G A missense_variant MODERATE c.1239G>A|p.Met413Ile S108
11 BAA08g17630 A08 14348940 C T missense_variant MODERATE c.2093C>T|p.Pro698Leu S88
12 BAA08g17630 A08 14349158 C T missense_variant MODERATE c.2311C>T|p.His771Tyr S237
13 BAA08g17630 A08 14349322 C T intron_variant MODIFIER c.2365-22C>T| S262
14 BAA08g17630 A08 14349746 G A missense_variant MODERATE c.2767G>A|p.Glu923Lys S246
15 BAA08g17630 A08 14349929 C T intron_variant MODIFIER c.2871+79C>T| S274
16 BAA08g17630 A08 14350402 C T intron_variant MODIFIER c.2871+552C>T| S205
17 BAA08g17630 A08 14350649 G A intron_variant MODIFIER c.2871+799G>A| S140
18 BAA08g17630 A08 14351193 C T intron_variant MODIFIER c.2871+1343C>T| S46
19 BAA08g17630 A08 14352216 C T intron_variant MODIFIER c.2872-2200C>T| S144
20 BAA08g17630 A08 14352364 C T intron_variant MODIFIER c.2872-2052C>T| S262
21 BAA08g17630 A08 14352561 G A intron_variant MODIFIER c.2872-1855G>A| S61
22 BAA08g17630 A08 14353080 G A intron_variant MODIFIER c.2872-1336G>A| S107
23 BAA08g17630 A08 14354466 C T synonymous_variant LOW c.2922C>T|p.Ile974Ile S270
24 BAA08g17630 A08 14354780 G T stop_gained HIGH c.2965G>T|p.Gly989* S215
25 BAA08g17630 A08 14354988 G A missense_variant MODERATE c.3110G>A|p.Arg1037Lys S116