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


Gene ID

Results: 1 - 46 of 46 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g07410 A07 16620407 G A upstream_gene_variant MODIFIER c.-4835G>A| S46
2 BAA07g07410 A07 16620499 C T upstream_gene_variant MODIFIER c.-4743C>T| S203
3 BAA07g07410 A07 16621696 G A upstream_gene_variant MODIFIER c.-3546G>A| S139
4 BAA07g07410 A07 16622379 G A upstream_gene_variant MODIFIER c.-2863G>A| S43
5 BAA07g07410 A07 16622448 C T upstream_gene_variant MODIFIER c.-2794C>T| S12
6 BAA07g07410 A07 16623385 T A upstream_gene_variant MODIFIER c.-1857T>A| S302
7 BAA07g07410 A07 16624037 G A upstream_gene_variant MODIFIER c.-1205G>A| S132
S89
8 BAA07g07410 A07 16624124 G A upstream_gene_variant MODIFIER c.-1118G>A| S142
9 BAA07g07410 A07 16624318 C T upstream_gene_variant MODIFIER c.-924C>T| S302
10 BAA07g07410 A07 16624409 C T upstream_gene_variant MODIFIER c.-833C>T| S136
11 BAA07g07410 A07 16624500 C T upstream_gene_variant MODIFIER c.-742C>T| S90
12 BAA07g07410 A07 16624685 G A upstream_gene_variant MODIFIER c.-557G>A| S62
13 BAA07g07410 A07 16624970 C T upstream_gene_variant MODIFIER c.-272C>T| S61
14 BAA07g07410 A07 16625354 C T missense_variant&splice_region_variant MODERATE c.113C>T|p.Ser38Phe S142
15 BAA07g07410 A07 16625638 C T intron_variant MODIFIER c.113+284C>T| S19
16 BAA07g07410 A07 16626277 G A intron_variant MODIFIER c.208+155G>A| S257
17 BAA07g07410 A07 16626672 G A intron_variant MODIFIER c.208+550G>A| S64
18 BAA07g07410 A07 16627197 G A intron_variant MODIFIER c.208+1075G>A| S245
19 BAA07g07410 A07 16627898 C T intron_variant MODIFIER c.208+1776C>T| S250
20 BAA07g07410 A07 16629544 C T intron_variant MODIFIER c.209-2687C>T| S100
21 BAA07g07410 A07 16629839 C T intron_variant MODIFIER c.209-2392C>T| S207
22 BAA07g07410 A07 16629997 C T intron_variant MODIFIER c.209-2234C>T| S230
23 BAA07g07410 A07 16630646 C T intron_variant MODIFIER c.209-1585C>T| S303
24 BAA07g07410 A07 16632099 C T intron_variant MODIFIER c.209-132C>T| S8
25 BAA07g07410 A07 16632273 C T missense_variant MODERATE c.251C>T|p.Ser84Phe S32