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


Gene ID

Results: 1 - 32 of 32 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g34100 A02 29237971 C T upstream_gene_variant MODIFIER c.-4602C>T| S212
2 BAA02g34100 A02 29243413 C T intron_variant MODIFIER c.195+197C>T| S1
S90
3 BAA02g34100 A02 29244361 G A intron_variant MODIFIER c.522+33G>A| S241
4 BAA02g34100 A02 29244772 G A missense_variant MODERATE c.713G>A|p.Arg238Lys S279
5 BAA02g34100 A02 29244794 G A synonymous_variant LOW c.735G>A|p.Leu245Leu S247
6 BAA02g34100 A02 29244820 G A missense_variant MODERATE c.761G>A|p.Arg254Lys S166
7 BAA02g34100 A02 29245015 C T intron_variant MODIFIER c.852+104C>T| S208
8 BAA02g34100 A02 29247247 C T intron_variant MODIFIER c.892+2040C>T| S203
9 BAA02g34100 A02 29247249 C T intron_variant MODIFIER c.892+2042C>T| S183
S198
10 BAA02g34100 A02 29248258 G A intron_variant MODIFIER c.892+3051G>A| S12
11 BAA02g34100 A02 29248263 C T intron_variant MODIFIER c.892+3056C>T| S108
12 BAA02g34100 A02 29249594 C T intron_variant MODIFIER c.892+4387C>T| S284
13 BAA02g34100 A02 29250171 C T intron_variant MODIFIER c.892+4964C>T| S140
14 BAA02g34100 A02 29250219 G A intron_variant MODIFIER c.892+5012G>A| S99
15 BAA02g34100 A02 29250938 C T intron_variant MODIFIER c.892+5731C>T| S105
S106
16 BAA02g34100 A02 29251241 T G intron_variant MODIFIER c.892+6034T>G| S162
S163
S204
S292
S297
S51
S57
S64
S71
17 BAA02g34100 A02 29254133 G A intron_variant MODIFIER c.893-6074G>A| S48
18 BAA02g34100 A02 29254394 G A intron_variant MODIFIER c.893-5813G>A| S133
19 BAA02g34100 A02 29257301 A T intron_variant MODIFIER c.893-2906A>T| S26
20 BAA02g34100 A02 29257492 G A intron_variant MODIFIER c.893-2715G>A| S256
21 BAA02g34100 A02 29258033 G A intron_variant MODIFIER c.893-2174G>A| S62
22 BAA02g34100 A02 29258303 C T intron_variant MODIFIER c.893-1904C>T| S182
23 BAA02g34100 A02 29259668 G A intron_variant MODIFIER c.893-539G>A| S45
24 BAA02g34100 A02 29259808 G A intron_variant MODIFIER c.893-399G>A| S56
25 BAA02g34100 A02 29261693 G A missense_variant MODERATE c.1180G>A|p.Glu394Lys S269