Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g37470 | A01 | 25001024 | G | A | upstream_gene_variant | MODIFIER | c.-4271G>A| |
S86 |
2 | BAA01g37470 | A01 | 25001452 | C | T | upstream_gene_variant | MODIFIER | c.-3843C>T| |
S74 |
3 | BAA01g37470 | A01 | 25001567 | C | T | upstream_gene_variant | MODIFIER | c.-3728C>T| |
S104 S52 |
4 | BAA01g37470 | A01 | 25005442 | G | A | missense_variant | MODERATE | c.70G>A|p.Ala24Thr |
S209 |
5 | BAA01g37470 | A01 | 25005804 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.205-1G>A| |
S95 |
6 | BAA01g37470 | A01 | 25006610 | C | T | missense_variant | MODERATE | c.1010C>T|p.Ser337Leu |
S59 |
7 | BAA01g37470 | A01 | 25007273 | C | T | intron_variant | MODIFIER | c.1032+641C>T| |
S46 |
8 | BAA01g37470 | A01 | 25008614 | C | T | intron_variant | MODIFIER | c.1033-1243C>T| |
S203 |
9 | BAA01g37470 | A01 | 25008800 | C | T | intron_variant | MODIFIER | c.1033-1057C>T| |
S77 |
10 | BAA01g37470 | A01 | 25008918 | C | T | intron_variant | MODIFIER | c.1033-939C>T| |
S230 |
11 | BAA01g37470 | A01 | 25009578 | T | A | intron_variant | MODIFIER | c.1033-279T>A| |
S210 |
12 | BAA01g37470 | A01 | 25009861 | G | A | missense_variant | MODERATE | c.1037G>A|p.Arg346Lys |
S263 |
13 | BAA01g37470 | A01 | 25009862 | G | A | synonymous_variant | LOW | c.1038G>A|p.Arg346Arg |
S283 |
14 | BAA01g37470 | A01 | 25009988 | G | A | intron_variant | MODIFIER | c.1152+12G>A| |
|
15 | BAA01g37470 | A01 | 25010038 | G | A | intron_variant | MODIFIER | c.1152+62G>A| |
S97 |
16 | BAA01g37470 | A01 | 25010115 | C | A | intron_variant | MODIFIER | c.1152+139C>A| |
S94 |
17 | BAA01g37470 | A01 | 25010275 | C | T | intron_variant | MODIFIER | c.1152+299C>T| |
S97 |
18 | BAA01g37470 | A01 | 25010848 | G | A | intron_variant | MODIFIER | c.1152+872G>A| |
S287 |
19 | BAA01g37470 | A01 | 25010980 | G | A | intron_variant | MODIFIER | c.1152+1004G>A| |
S290 |
20 | BAA01g37470 | A01 | 25011305 | C | T | intron_variant | MODIFIER | c.1152+1329C>T| |
S10 |
21 | BAA01g37470 | A01 | 25011385 | C | T | intron_variant | MODIFIER | c.1152+1409C>T| |
S228 |
22 | BAA01g37470 | A01 | 25012927 | C | T | intron_variant | MODIFIER | c.1153-2367C>T| |
S249 |
23 | BAA01g37470 | A01 | 25013639 | G | A | intron_variant | MODIFIER | c.1153-1655G>A| |
S6 |
24 | BAA01g37470 | A01 | 25014144 | C | T | intron_variant | MODIFIER | c.1153-1150C>T| |
S293 |
25 | BAA01g37470 | A01 | 25015463 | C | T | intron_variant | MODIFIER | c.1297+25C>T| |
S17 |