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 BAA09g55520 A09 55637598 G A downstream_gene_variant MODIFIER c.*4519C>T| S10
2 BAA09g55520 A09 55638497 C T downstream_gene_variant MODIFIER c.*3620G>A| S206
S26
3 BAA09g55520 A09 55639087 G A downstream_gene_variant MODIFIER c.*3030C>T| S204
4 BAA09g55520 A09 55639090 C T downstream_gene_variant MODIFIER c.*3027G>A| S80
5 BAA09g55520 A09 55639335 C T downstream_gene_variant MODIFIER c.*2782G>A| S64
6 BAA09g55520 A09 55639406 G A downstream_gene_variant MODIFIER c.*2711C>T| S221
7 BAA09g55520 A09 55640171 C T downstream_gene_variant MODIFIER c.*1946G>A| S138
8 BAA09g55520 A09 55640208 C T downstream_gene_variant MODIFIER c.*1909G>A| S168
9 BAA09g55520 A09 55640306 G A downstream_gene_variant MODIFIER c.*1811C>T| S270
10 BAA09g55520 A09 55640666 C T downstream_gene_variant MODIFIER c.*1451G>A| S303
11 BAA09g55520 A09 55640963 C T downstream_gene_variant MODIFIER c.*1154G>A| S120
12 BAA09g55520 A09 55641375 C T downstream_gene_variant MODIFIER c.*742G>A| S306
13 BAA09g55520 A09 55641734 C T downstream_gene_variant MODIFIER c.*383G>A| S203
14 BAA09g55520 A09 55642746 C T intron_variant MODIFIER c.1433+28G>A| S45
15 BAA09g55520 A09 55643788 C T missense_variant MODERATE c.874G>A|p.Val292Ile S169
16 BAA09g55520 A09 55644199 C T intron_variant MODIFIER c.778+113G>A| S278
17 BAA09g55520 A09 55645863 C T intron_variant MODIFIER c.503+294G>A| S35
18 BAA09g55520 A09 55646073 C T intron_variant MODIFIER c.503+84G>A| S140
19 BAA09g55520 A09 55648242 C T upstream_gene_variant MODIFIER c.-1406G>A| S301
S304
20 BAA09g55520 A09 55649353 C T upstream_gene_variant MODIFIER c.-2517G>A| S274
21 BAA09g55520 A09 55649509 G A upstream_gene_variant MODIFIER c.-2673C>T| S180
22 BAA09g55520 A09 55649673 C T upstream_gene_variant MODIFIER c.-2837G>A| S139
23 BAA09g55520 A09 55650577 G A upstream_gene_variant MODIFIER c.-3741C>T| S112