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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g05580 A08 4250057 G A downstream_gene_variant MODIFIER c.*4246C>T| S165
2 BAA08g05580 A08 4250858 C T downstream_gene_variant MODIFIER c.*3445G>A| S134
3 BAA08g05580 A08 4251494 C T downstream_gene_variant MODIFIER c.*2809G>A| S15
S3
4 BAA08g05580 A08 4252880 G A downstream_gene_variant MODIFIER c.*1423C>T| S257
5 BAA08g05580 A08 4253183 C T downstream_gene_variant MODIFIER c.*1120G>A| S233
6 BAA08g05580 A08 4253483 G A downstream_gene_variant MODIFIER c.*820C>T| S202
7 BAA08g05580 A08 4253489 C T downstream_gene_variant MODIFIER c.*814G>A| S284
8 BAA08g05580 A08 4254204 C T downstream_gene_variant MODIFIER c.*99G>A| S34
9 BAA08g05580 A08 4255272 C T intron_variant MODIFIER c.1440+227G>A| S168
S64
10 BAA08g05580 A08 4255404 C T intron_variant MODIFIER c.1440+95G>A| S213
11 BAA08g05580 A08 4255787 G A synonymous_variant LOW c.1260C>T|p.Asn420Asn S255
12 BAA08g05580 A08 4256507 G A synonymous_variant LOW c.540C>T|p.Ser180Ser S202
13 BAA08g05580 A08 4256766 C T missense_variant MODERATE c.281G>A|p.Gly94Glu S111
14 BAA08g05580 A08 4256878 C T missense_variant MODERATE c.169G>A|p.Ala57Thr S142
15 BAA08g05580 A08 4256985 G A missense_variant MODERATE c.62C>T|p.Ser21Phe S202
16 BAA08g05580 A08 4257259 C T upstream_gene_variant MODIFIER c.-213G>A| S308
17 BAA08g05580 A08 4257440 C T upstream_gene_variant MODIFIER c.-394G>A| S66
18 BAA08g05580 A08 4257645 G A upstream_gene_variant MODIFIER c.-599C>T| S117
19 BAA08g05580 A08 4258156 G A upstream_gene_variant MODIFIER c.-1110C>T| S111
20 BAA08g05580 A08 4260296 C T upstream_gene_variant MODIFIER c.-3250G>A| S287
21 BAA08g05580 A08 4260903 G A upstream_gene_variant MODIFIER c.-3857C>T| S115
22 BAA08g05580 A08 4261555 C T upstream_gene_variant MODIFIER c.-4509G>A| S206
S26
23 BAA08g05580 A08 4261807 G A upstream_gene_variant MODIFIER c.-4761C>T| S263