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


Gene ID

Results: 1 - 27 of 27 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g10610 A10 12351225 G A upstream_gene_variant MODIFIER c.-4333G>A| S295
2 BAA10g10610 A10 12351274 G A upstream_gene_variant MODIFIER c.-4284G>A| S89
3 BAA10g10610 A10 12351436 G A upstream_gene_variant MODIFIER c.-4122G>A| S303
4 BAA10g10610 A10 12351701 G A upstream_gene_variant MODIFIER c.-3857G>A| S68
5 BAA10g10610 A10 12352254 C T upstream_gene_variant MODIFIER c.-3304C>T| S274
6 BAA10g10610 A10 12352450 C T upstream_gene_variant MODIFIER c.-3108C>T| S28
7 BAA10g10610 A10 12353231 G A upstream_gene_variant MODIFIER c.-2327G>A| S276
8 BAA10g10610 A10 12353243 C T upstream_gene_variant MODIFIER c.-2315C>T| S276
9 BAA10g10610 A10 12353418 T G upstream_gene_variant MODIFIER c.-2140T>G| S35
10 BAA10g10610 A10 12353766 G A upstream_gene_variant MODIFIER c.-1792G>A| S205
S245
11 BAA10g10610 A10 12353913 G A upstream_gene_variant MODIFIER c.-1645G>A| S259
12 BAA10g10610 A10 12356131 G A missense_variant MODERATE c.493G>A|p.Ala165Thr S172
S217
13 BAA10g10610 A10 12356477 C T missense_variant MODERATE c.839C>T|p.Pro280Leu S23
14 BAA10g10610 A10 12356503 G A missense_variant MODERATE c.865G>A|p.Gly289Arg S161
15 BAA10g10610 A10 12356654 G A missense_variant MODERATE c.1016G>A|p.Gly339Glu S241
16 BAA10g10610 A10 12356948 C T intron_variant MODIFIER c.1227-63C>T| S149
17 BAA10g10610 A10 12357078 G A missense_variant MODERATE c.1294G>A|p.Gly432Ser S134
18 BAA10g10610 A10 12357248 C T synonymous_variant LOW c.1464C>T|p.Arg488Arg S282
19 BAA10g10610 A10 12357508 G A missense_variant MODERATE c.1724G>A|p.Arg575Gln S105
S106
20 BAA10g10610 A10 12357896 A T missense_variant MODERATE c.2112A>T|p.Arg704Ser S181
21 BAA10g10610 A10 12358514 C T downstream_gene_variant MODIFIER c.*612C>T| S247
22 BAA10g10610 A10 12358688 C T downstream_gene_variant MODIFIER c.*786C>T| S142
23 BAA10g10610 A10 12358729 G A downstream_gene_variant MODIFIER c.*827G>A| S228
24 BAA10g10610 A10 12358739 T C downstream_gene_variant MODIFIER c.*837T>C| S114
25 BAA10g10610 A10 12358908 C T downstream_gene_variant MODIFIER c.*1006C>T| S98