Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g14080 | A04 | 19293069 | C | T | downstream_gene_variant | MODIFIER | c.*4085G>A| |
S148 S30 |
2 | BAA04g14080 | A04 | 19294952 | C | A | downstream_gene_variant | MODIFIER | c.*2202G>T| |
S265 |
3 | BAA04g14080 | A04 | 19295538 | G | A | downstream_gene_variant | MODIFIER | c.*1616C>T| |
S58 |
4 | BAA04g14080 | A04 | 19295730 | G | A | downstream_gene_variant | MODIFIER | c.*1424C>T| |
S211 S227 |
5 | BAA04g14080 | A04 | 19296408 | C | T | downstream_gene_variant | MODIFIER | c.*746G>A| |
S67 |
6 | BAA04g14080 | A04 | 19297306 | G | T | splice_region_variant&intron_variant | LOW | c.1573-3C>A| |
S104 S111 S173 S208 S90 |
7 | BAA04g14080 | A04 | 19297481 | C | T | missense_variant | MODERATE | c.1475G>A|p.Ser492Asn |
S197 |
8 | BAA04g14080 | A04 | 19297621 | G | A | missense_variant | MODERATE | c.1427C>T|p.Pro476Leu |
S150 |
9 | BAA04g14080 | A04 | 19297702 | G | A | missense_variant | MODERATE | c.1346C>T|p.Pro449Leu |
S293 |
10 | BAA04g14080 | A04 | 19297944 | C | T | missense_variant | MODERATE | c.1199G>A|p.Gly400Asp |
S205 |
11 | BAA04g14080 | A04 | 19298025 | G | A | missense_variant | MODERATE | c.1118C>T|p.Ser373Leu |
S158 |
12 | BAA04g14080 | A04 | 19298191 | C | T | missense_variant | MODERATE | c.952G>A|p.Ala318Thr |
S95 |
13 | BAA04g14080 | A04 | 19298414 | C | T | synonymous_variant | LOW | c.729G>A|p.Thr243Thr |
S25 |
14 | BAA04g14080 | A04 | 19299145 | G | A | synonymous_variant | LOW | c.75C>T|p.Asp25Asp |
|
15 | BAA04g14080 | A04 | 19300592 | G | A | upstream_gene_variant | MODIFIER | c.-1373C>T| |
S83 S88 |
16 | BAA04g14080 | A04 | 19300953 | G | A | upstream_gene_variant | MODIFIER | c.-1734C>T| |
S109 |
17 | BAA04g14080 | A04 | 19304027 | G | A | upstream_gene_variant | MODIFIER | c.-4808C>T| |
S238 |