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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g18390 A10 17216118 G A upstream_gene_variant MODIFIER c.-2679G>A| S35
2 BAA10g18390 A10 17216614 C T upstream_gene_variant MODIFIER c.-2183C>T| S180
3 BAA10g18390 A10 17216645 C T upstream_gene_variant MODIFIER c.-2152C>T| S156
4 BAA10g18390 A10 17216806 G A upstream_gene_variant MODIFIER c.-1991G>A| S69
5 BAA10g18390 A10 17217163 C T upstream_gene_variant MODIFIER c.-1634C>T| S256
6 BAA10g18390 A10 17218572 G A upstream_gene_variant MODIFIER c.-225G>A| S176
7 BAA10g18390 A10 17219344 G A missense_variant MODERATE c.372G>A|p.Met124Ile S38
8 BAA10g18390 A10 17219365 G A synonymous_variant LOW c.393G>A|p.Ala131Ala S166
9 BAA10g18390 A10 17220193 C T synonymous_variant LOW c.883C>T|p.Leu295Leu S163
10 BAA10g18390 A10 17220448 G A missense_variant MODERATE c.1073G>A|p.Arg358Gln S279
11 BAA10g18390 A10 17220937 C T synonymous_variant LOW c.1284C>T|p.Leu428Leu S144
12 BAA10g18390 A10 17221521 C T synonymous_variant LOW c.1638C>T|p.Pro546Pro S51
13 BAA10g18390 A10 17221677 C T synonymous_variant LOW c.1693C>T|p.Leu565Leu S48
14 BAA10g18390 A10 17221701 C T missense_variant MODERATE c.1717C>T|p.Pro573Ser S170
15 BAA10g18390 A10 17222757 G A downstream_gene_variant MODIFIER c.*200G>A| S15
S3
16 BAA10g18390 A10 17223163 C T downstream_gene_variant MODIFIER c.*606C>T| S186
17 BAA10g18390 A10 17223166 C T downstream_gene_variant MODIFIER c.*609C>T| S70
18 BAA10g18390 A10 17224194 C T downstream_gene_variant MODIFIER c.*1637C>T| S23
19 BAA10g18390 A10 17226204 G A downstream_gene_variant MODIFIER c.*3647G>A| S219
S236
S279
20 BAA10g18390 A10 17226335 G T downstream_gene_variant MODIFIER c.*3778G>T| S177
S233