Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g40820 | A07 | 36052946 | G | A | upstream_gene_variant | MODIFIER | c.-83G>A| |
S33 |
2 | BAA07g40820 | A07 | 36053290 | C | T | intron_variant | MODIFIER | c.55-123C>T| |
S159 S243 |
3 | BAA07g40820 | A07 | 36053336 | G | A | intron_variant | MODIFIER | c.55-77G>A| |
S163 |
4 | BAA07g40820 | A07 | 36053526 | C | T | intron_variant | MODIFIER | c.141+27C>T| |
S179 |
5 | BAA07g40820 | A07 | 36053733 | G | A | intron_variant | MODIFIER | c.232-53G>A| |
S231 |
6 | BAA07g40820 | A07 | 36054283 | C | T | intron_variant | MODIFIER | c.438+203C>T| |
S252 |
7 | BAA07g40820 | A07 | 36055040 | C | T | missense_variant | MODERATE | c.479C>T|p.Ser160Phe |
S124 |
8 | BAA07g40820 | A07 | 36055294 | G | A | missense_variant | MODERATE | c.733G>A|p.Val245Ile |
S296 |
9 | BAA07g40820 | A07 | 36055723 | C | T | missense_variant | MODERATE | c.1162C>T|p.His388Tyr |
S79 S91 |
10 | BAA07g40820 | A07 | 36056184 | G | A | synonymous_variant | LOW | c.1623G>A|p.Ala541Ala |
S289 S290 |
11 | BAA07g40820 | A07 | 36056650 | G | A | missense_variant | MODERATE | c.2089G>A|p.Gly697Arg |
S69 |
12 | BAA07g40820 | A07 | 36056877 | C | T | synonymous_variant | LOW | c.2316C>T|p.Ser772Ser |
S190 |
13 | BAA07g40820 | A07 | 36057987 | C | T | missense_variant | MODERATE | c.2827C>T|p.Pro943Ser |
S19 |
14 | BAA07g40820 | A07 | 36058353 | G | A | missense_variant | MODERATE | c.3115G>A|p.Glu1039Lys |
S17 |
15 | BAA07g40820 | A07 | 36058648 | C | T | downstream_gene_variant | MODIFIER | c.*185C>T| |
S177 |
16 | BAA07g40820 | A07 | 36058829 | C | T | downstream_gene_variant | MODIFIER | c.*366C>T| |
S165 |
17 | BAA07g40820 | A07 | 36059056 | C | T | downstream_gene_variant | MODIFIER | c.*593C>T| |
S168 |