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


Gene ID

Results: 1 - 26 of 26 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g05140 A10 2654430 G A upstream_gene_variant MODIFIER c.-1627G>A| S66
2 BAA10g05140 A10 2654840 C T upstream_gene_variant MODIFIER c.-1217C>T| S174
S27
3 BAA10g05140 A10 2654923 G A upstream_gene_variant MODIFIER c.-1134G>A| S280
4 BAA10g05140 A10 2655677 C T upstream_gene_variant MODIFIER c.-380C>T| S10
5 BAA10g05140 A10 2657110 C T missense_variant MODERATE c.805C>T|p.Pro269Ser S37
6 BAA10g05140 A10 2657441 G A missense_variant&splice_region_variant MODERATE c.974G>A|p.Arg325Lys S43
7 BAA10g05140 A10 2657955 G A synonymous_variant LOW c.1227G>A|p.Lys409Lys S129
8 BAA10g05140 A10 2658313 G A splice_acceptor_variant&intron_variant HIGH c.1435-1G>A| S192
9 BAA10g05140 A10 2658380 G A missense_variant MODERATE c.1501G>A|p.Gly501Arg S296
10 BAA10g05140 A10 2660171 C T intron_variant MODIFIER c.1788+1352C>T| S104
S52
11 BAA10g05140 A10 2660213 C T intron_variant MODIFIER c.1788+1394C>T| S37
12 BAA10g05140 A10 2662111 C T intron_variant MODIFIER c.1789-376C>T| S206
S26
13 BAA10g05140 A10 2663004 G A downstream_gene_variant MODIFIER c.*275G>A| S125
14 BAA10g05140 A10 2663419 C T downstream_gene_variant MODIFIER c.*690C>T| S210
15 BAA10g05140 A10 2663685 G A downstream_gene_variant MODIFIER c.*956G>A| S95
16 BAA10g05140 A10 2664110 C T downstream_gene_variant MODIFIER c.*1381C>T| S165
17 BAA10g05140 A10 2664262 C T downstream_gene_variant MODIFIER c.*1533C>T| S68
18 BAA10g05140 A10 2664585 C T downstream_gene_variant MODIFIER c.*1856C>T| S202
19 BAA10g05140 A10 2664607 C T downstream_gene_variant MODIFIER c.*1878C>T| S23
20 BAA10g05140 A10 2664640 G A downstream_gene_variant MODIFIER c.*1911G>A| S12
21 BAA10g05140 A10 2664701 G A downstream_gene_variant MODIFIER c.*1972G>A| S20
22 BAA10g05140 A10 2664908 G A downstream_gene_variant MODIFIER c.*2179G>A| S216
23 BAA10g05140 A10 2665545 G A downstream_gene_variant MODIFIER c.*2816G>A| S192
24 BAA10g05140 A10 2666197 C T downstream_gene_variant MODIFIER c.*3468C>T| S56
25 BAA10g05140 A10 2666735 C T downstream_gene_variant MODIFIER c.*4006C>T| S79
S91