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


Gene ID

Results: 1 - 28 of 28 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g01330 A07 926985 C T downstream_gene_variant MODIFIER c.*3685G>A| S133
2 BAA07g01330 A07 927095 G A downstream_gene_variant MODIFIER c.*3575C>T| S83
S88
3 BAA07g01330 A07 930008 G A downstream_gene_variant MODIFIER c.*662C>T| S82
S92
4 BAA07g01330 A07 932609 G A intron_variant MODIFIER c.966-1897C>T| S238
5 BAA07g01330 A07 933240 G A intron_variant MODIFIER c.966-2528C>T| S268
6 BAA07g01330 A07 933384 C T intron_variant MODIFIER c.966-2672G>A| S53
7 BAA07g01330 A07 934013 C T intron_variant MODIFIER c.966-3301G>A| S213
8 BAA07g01330 A07 934688 C T intron_variant MODIFIER c.966-3976G>A| S207
9 BAA07g01330 A07 934935 C T intron_variant MODIFIER c.966-4223G>A| S247
10 BAA07g01330 A07 936077 C T intron_variant MODIFIER c.966-5365G>A| S203
11 BAA07g01330 A07 937066 C T intron_variant MODIFIER c.965+5972G>A| S263
12 BAA07g01330 A07 937568 G A intron_variant MODIFIER c.965+5470C>T| S151
13 BAA07g01330 A07 937844 C T intron_variant MODIFIER c.965+5194G>A| S265
14 BAA07g01330 A07 937890 G A intron_variant MODIFIER c.965+5148C>T| S62
15 BAA07g01330 A07 938060 C T intron_variant MODIFIER c.965+4978G>A| S85
16 BAA07g01330 A07 938264 G A intron_variant MODIFIER c.965+4774C>T| S294
S81
S85
17 BAA07g01330 A07 938887 G A intron_variant MODIFIER c.965+4151C>T| S262
18 BAA07g01330 A07 944871 G A missense_variant MODERATE c.245C>T|p.Pro82Leu S192
19 BAA07g01330 A07 946823 C T upstream_gene_variant MODIFIER c.-1257G>A| S90
20 BAA07g01330 A07 947053 C T upstream_gene_variant MODIFIER c.-1487G>A| S142
21 BAA07g01330 A07 948053 C T upstream_gene_variant MODIFIER c.-2487G>A| S8
22 BAA07g01330 A07 948215 C T upstream_gene_variant MODIFIER c.-2649G>A| S142
23 BAA07g01330 A07 948968 C T upstream_gene_variant MODIFIER c.-3402G>A| S231
24 BAA07g01330 A07 949300 G A upstream_gene_variant MODIFIER c.-3734C>T| S199
25 BAA07g01330 A07 950010 C T upstream_gene_variant MODIFIER c.-4444G>A| S169