Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g37960 | A09 | 46018305 | G | A | downstream_gene_variant | MODIFIER | c.*3106C>T| |
S151 S263 |
2 | BAA09g37960 | A09 | 46018391 | G | A | downstream_gene_variant | MODIFIER | c.*3020C>T| |
S107 |
3 | BAA09g37960 | A09 | 46019071 | G | A | downstream_gene_variant | MODIFIER | c.*2340C>T| |
S221 |
4 | BAA09g37960 | A09 | 46019141 | C | T | downstream_gene_variant | MODIFIER | c.*2270G>A| |
S40 |
5 | BAA09g37960 | A09 | 46021362 | G | A | downstream_gene_variant | MODIFIER | c.*49C>T| |
S134 |
6 | BAA09g37960 | A09 | 46022033 | C | T | missense_variant | MODERATE | c.3077G>A|p.Gly1026Glu |
S77 S82 |
7 | BAA09g37960 | A09 | 46022185 | A | T | missense_variant | MODERATE | c.2925T>A|p.His975Gln |
S82 |
8 | BAA09g37960 | A09 | 46022462 | G | A | missense_variant | MODERATE | c.2648C>T|p.Pro883Leu |
S280 |
9 | BAA09g37960 | A09 | 46023271 | C | T | synonymous_variant | LOW | c.2103G>A|p.Pro701Pro |
S153 |
10 | BAA09g37960 | A09 | 46023338 | C | T | missense_variant | MODERATE | c.2036G>A|p.Gly679Glu |
S123 |
11 | BAA09g37960 | A09 | 46024056 | C | T | intron_variant | MODIFIER | c.1477-159G>A| |
S306 S308 |
12 | BAA09g37960 | A09 | 46024365 | G | A | intron_variant | MODIFIER | c.1477-468C>T| |
S265 |
13 | BAA09g37960 | A09 | 46024715 | G | A | intron_variant | MODIFIER | c.1477-818C>T| |
S262 |
14 | BAA09g37960 | A09 | 46025627 | C | T | intron_variant | MODIFIER | c.1477-1730G>A| |
S219 S72 |
15 | BAA09g37960 | A09 | 46026047 | G | A | intron_variant | MODIFIER | c.1477-2150C>T| |
S264 |
16 | BAA09g37960 | A09 | 46026050 | C | T | intron_variant | MODIFIER | c.1477-2153G>A| |
S140 |
17 | BAA09g37960 | A09 | 46027570 | G | A | intron_variant | MODIFIER | c.1476+3517C>T| |
S148 S210 |
18 | BAA09g37960 | A09 | 46027621 | G | A | intron_variant | MODIFIER | c.1476+3466C>T| |
S305 |
19 | BAA09g37960 | A09 | 46029103 | G | A | intron_variant | MODIFIER | c.1476+1984C>T| |
S177 |
20 | BAA09g37960 | A09 | 46029695 | C | T | intron_variant | MODIFIER | c.1476+1392G>A| |
S298 |
21 | BAA09g37960 | A09 | 46030433 | C | T | intron_variant | MODIFIER | c.1476+654G>A| |
S140 |
22 | BAA09g37960 | A09 | 46030548 | A | C | intron_variant | MODIFIER | c.1476+539T>G| |
S6 |
23 | BAA09g37960 | A09 | 46031338 | C | T | missense_variant | MODERATE | c.1225G>A|p.Val409Ile |
S50 |
24 | BAA09g37960 | A09 | 46033540 | G | A | upstream_gene_variant | MODIFIER | c.-124C>T| |
S57 |
25 | BAA09g37960 | A09 | 46034288 | C | T | upstream_gene_variant | MODIFIER | c.-872G>A| |
S6 |