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


Gene ID

Results: 1 - 25 of 25 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g07160 A10 3978851 G A upstream_gene_variant MODIFIER c.-3891G>A| S13
2 BAA10g07160 A10 3983222 C T intron_variant MODIFIER c.300+181C>T| S286
3 BAA10g07160 A10 3985561 G A missense_variant MODERATE c.846G>A|p.Met282Ile S290
4 BAA10g07160 A10 3986444 G A intron_variant MODIFIER c.1106+623G>A| S284
5 BAA10g07160 A10 3986466 G A intron_variant MODIFIER c.1106+645G>A| S128
6 BAA10g07160 A10 3987324 C T intron_variant MODIFIER c.1221+76C>T| S142
7 BAA10g07160 A10 3987417 G A intron_variant MODIFIER c.1222-42G>A| S236
8 BAA10g07160 A10 3987919 C T intron_variant MODIFIER c.1624+58C>T| S135
9 BAA10g07160 A10 3988512 G A intron_variant MODIFIER c.1624+651G>A| S245
10 BAA10g07160 A10 3988536 G A intron_variant MODIFIER c.1624+675G>A| S262
11 BAA10g07160 A10 3988575 C T intron_variant MODIFIER c.1624+714C>T| S19
12 BAA10g07160 A10 3988798 G A intron_variant MODIFIER c.1625-831G>A| S55
13 BAA10g07160 A10 3989591 C T intron_variant MODIFIER c.1625-38C>T| S246
14 BAA10g07160 A10 3990612 G A missense_variant MODERATE c.2245G>A|p.Gly749Arg S202
15 BAA10g07160 A10 3991026 G A missense_variant MODERATE c.2572G>A|p.Val858Met S236
16 BAA10g07160 A10 3991472 C T intron_variant MODIFIER c.2695+323C>T| S199
17 BAA10g07160 A10 3991843 C T intron_variant MODIFIER c.2696-496C>T| S243
S299
18 BAA10g07160 A10 3992172 G A intron_variant MODIFIER c.2696-167G>A| S208
S219
19 BAA10g07160 A10 3993312 C G downstream_gene_variant MODIFIER c.*500C>G| S109
20 BAA10g07160 A10 3993575 C T downstream_gene_variant MODIFIER c.*763C>T| S199
21 BAA10g07160 A10 3993846 C T downstream_gene_variant MODIFIER c.*1034C>T| S271
22 BAA10g07160 A10 3994757 C T downstream_gene_variant MODIFIER c.*1945C>T| S117
23 BAA10g07160 A10 3995993 G A downstream_gene_variant MODIFIER c.*3181G>A| S178
24 BAA10g07160 A10 3996589 G A downstream_gene_variant MODIFIER c.*3777G>A| S4
25 BAA10g07160 A10 3997690 C T downstream_gene_variant MODIFIER c.*4878C>T| S11
S189