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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g06950 A08 5691908 G A upstream_gene_variant MODIFIER c.-4820G>A| S98
2 BAA08g06950 A08 5692045 G A upstream_gene_variant MODIFIER c.-4683G>A| S38
3 BAA08g06950 A08 5693607 G A upstream_gene_variant MODIFIER c.-3121G>A| S278
4 BAA08g06950 A08 5693778 A C upstream_gene_variant MODIFIER c.-2950A>C| S212
5 BAA08g06950 A08 5694450 G A upstream_gene_variant MODIFIER c.-2278G>A| S161
6 BAA08g06950 A08 5694627 C T upstream_gene_variant MODIFIER c.-2101C>T| S155
S211
7 BAA08g06950 A08 5695016 G A upstream_gene_variant MODIFIER c.-1712G>A| S242
8 BAA08g06950 A08 5695850 C T upstream_gene_variant MODIFIER c.-878C>T| S80
9 BAA08g06950 A08 5696134 G A upstream_gene_variant MODIFIER c.-594G>A| S301
S304
10 BAA08g06950 A08 5696780 C T missense_variant MODERATE c.53C>T|p.Thr18Ile S157
S163
11 BAA08g06950 A08 5696826 C T synonymous_variant LOW c.99C>T|p.Ser33Ser S63
12 BAA08g06950 A08 5697216 C T intron_variant MODIFIER c.294+195C>T| S301
S304
13 BAA08g06950 A08 5697253 G A intron_variant MODIFIER c.294+232G>A| S98
14 BAA08g06950 A08 5698363 G C intron_variant MODIFIER c.294+1342G>C| S18
15 BAA08g06950 A08 5700840 G A intron_variant MODIFIER c.295-235G>A| S181
16 BAA08g06950 A08 5700868 G A intron_variant MODIFIER c.295-207G>A| S200
17 BAA08g06950 A08 5700959 G A intron_variant MODIFIER c.295-116G>A| S218
18 BAA08g06950 A08 5701613 G A intron_variant MODIFIER c.439-206G>A| S117
19 BAA08g06950 A08 5706403 G A downstream_gene_variant MODIFIER c.*4441G>A| S288