Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g16740 | A09 | 9831151 | G | T | upstream_gene_variant | MODIFIER | c.-4734G>T| |
S37 |
2 | BAA09g16740 | A09 | 9831605 | C | T | upstream_gene_variant | MODIFIER | c.-4280C>T| |
S13 |
3 | BAA09g16740 | A09 | 9831623 | G | A | upstream_gene_variant | MODIFIER | c.-4262G>A| |
S99 |
4 | BAA09g16740 | A09 | 9831625 | G | A | upstream_gene_variant | MODIFIER | c.-4260G>A| |
S182 |
5 | BAA09g16740 | A09 | 9832523 | C | T | upstream_gene_variant | MODIFIER | c.-3362C>T| |
S138 |
6 | BAA09g16740 | A09 | 9832648 | G | A | upstream_gene_variant | MODIFIER | c.-3237G>A| |
S88 |
7 | BAA09g16740 | A09 | 9832777 | C | T | upstream_gene_variant | MODIFIER | c.-3108C>T| |
S231 |
8 | BAA09g16740 | A09 | 9833255 | C | T | upstream_gene_variant | MODIFIER | c.-2630C>T| |
S48 |
9 | BAA09g16740 | A09 | 9833402 | C | T | upstream_gene_variant | MODIFIER | c.-2483C>T| |
S13 |
10 | BAA09g16740 | A09 | 9833855 | G | A | upstream_gene_variant | MODIFIER | c.-2030G>A| |
S67 |
11 | BAA09g16740 | A09 | 9834404 | G | A | upstream_gene_variant | MODIFIER | c.-1481G>A| |
S225 S73 |
12 | BAA09g16740 | A09 | 9834960 | G | A | upstream_gene_variant | MODIFIER | c.-925G>A| |
S159 S243 S299 |
13 | BAA09g16740 | A09 | 9835407 | C | T | upstream_gene_variant | MODIFIER | c.-478C>T| |
S283 |
14 | BAA09g16740 | A09 | 9835879 | G | A | upstream_gene_variant | MODIFIER | c.-6G>A| |
S277 |
15 | BAA09g16740 | A09 | 9836052 | G | A | intron_variant | MODIFIER | c.84+84G>A| |
S249 |
16 | BAA09g16740 | A09 | 9836791 | C | T | missense_variant | MODERATE | c.461C>T|p.Ala154Val |
S85 |
17 | BAA09g16740 | A09 | 9837152 | C | T | intron_variant | MODIFIER | c.630-73C>T| |
S135 |
18 | BAA09g16740 | A09 | 9837235 | C | T | missense_variant | MODERATE | c.640C>T|p.Pro214Ser |
S168 |
19 | BAA09g16740 | A09 | 9837637 | G | A | missense_variant | MODERATE | c.868G>A|p.Asp290Asn |
S162 |
20 | BAA09g16740 | A09 | 9837655 | G | A | missense_variant | MODERATE | c.886G>A|p.Glu296Lys |
S1 S90 |
21 | BAA09g16740 | A09 | 9837667 | C | T | synonymous_variant | LOW | c.898C>T|p.Leu300Leu |
S213 |
22 | BAA09g16740 | A09 | 9837814 | G | A | splice_region_variant&intron_variant | LOW | c.922-4G>A| |
S207 |
23 | BAA09g16740 | A09 | 9838456 | G | A | missense_variant | MODERATE | c.1163G>A|p.Ser388Asn |
S210 |
24 | BAA09g16740 | A09 | 9839348 | G | A | downstream_gene_variant | MODIFIER | c.*705G>A| |
S33 |