Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g24840 | A09 | 15909884 | G | A | upstream_gene_variant | MODIFIER | c.-4879G>A| |
S221 |
2 | BAA09g24840 | A09 | 15910705 | G | A | upstream_gene_variant | MODIFIER | c.-4058G>A| |
S45 |
3 | BAA09g24840 | A09 | 15911209 | C | T | upstream_gene_variant | MODIFIER | c.-3554C>T| |
S56 |
4 | BAA09g24840 | A09 | 15915067 | G | A | missense_variant | MODERATE | c.181G>A|p.Gly61Ser |
S20 |
5 | BAA09g24840 | A09 | 15915161 | T | C | missense_variant | MODERATE | c.275T>C|p.Leu92Ser |
S175 |
6 | BAA09g24840 | A09 | 15915312 | G | A | synonymous_variant | LOW | c.426G>A|p.Lys142Lys |
S202 |
7 | BAA09g24840 | A09 | 15916108 | C | T | missense_variant | MODERATE | c.935C>T|p.Pro312Leu |
S104 S52 |
8 | BAA09g24840 | A09 | 15918223 | C | T | missense_variant | MODERATE | c.1927C>T|p.Pro643Ser |
S76 |
9 | BAA09g24840 | A09 | 15919464 | C | T | synonymous_variant | LOW | c.2811C>T|p.Asp937Asp |
S277 |
10 | BAA09g24840 | A09 | 15920369 | C | T | intron_variant | MODIFIER | c.3408+13C>T| |
S188 |
11 | BAA09g24840 | A09 | 15920459 | C | T | intron_variant | MODIFIER | c.3409-17C>T| |
S278 |
12 | BAA09g24840 | A09 | 15920677 | G | A | missense_variant | MODERATE | c.3610G>A|p.Asp1204Asn |
S259 |
13 | BAA09g24840 | A09 | 15920880 | C | T | intron_variant | MODIFIER | c.3670-27C>T| |
S148 S210 |
14 | BAA09g24840 | A09 | 15920985 | C | T | intron_variant | MODIFIER | c.3732+16C>T| |
S151 S263 |
15 | BAA09g24840 | A09 | 15922382 | A | G | downstream_gene_variant | MODIFIER | c.*1234A>G| |
S64 |
16 | BAA09g24840 | A09 | 15923396 | G | A | downstream_gene_variant | MODIFIER | c.*2248G>A| |
S202 |
17 | BAA09g24840 | A09 | 15923593 | G | A | downstream_gene_variant | MODIFIER | c.*2445G>A| |
S189 |
18 | BAA09g24840 | A09 | 15924177 | C | T | downstream_gene_variant | MODIFIER | c.*3029C>T| |
S28 |
19 | BAA09g24840 | A09 | 15925289 | C | T | downstream_gene_variant | MODIFIER | c.*4141C>T| |
S168 |
20 | BAA09g24840 | A09 | 15926028 | G | A | downstream_gene_variant | MODIFIER | c.*4880G>A| |
S194 |
21 | BAA09g24840 | A09 | 15926140 | G | A | downstream_gene_variant | MODIFIER | c.*4992G>A| |
S210 |