Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07160 | A10 | 3978851 | G | A | upstream_gene_variant | MODIFIER | c.-3891G>A| |
S13 |
2 | BAA10g07160 | A10 | 3983222 | C | T | intron_variant | MODIFIER | c.300+181C>T| |
S286 |
3 | BAA10g07160 | A10 | 3985561 | G | A | missense_variant | MODERATE | c.846G>A|p.Met282Ile |
S290 |
4 | BAA10g07160 | A10 | 3986444 | G | A | intron_variant | MODIFIER | c.1106+623G>A| |
S284 |
5 | BAA10g07160 | A10 | 3986466 | G | A | intron_variant | MODIFIER | c.1106+645G>A| |
S128 |
6 | BAA10g07160 | A10 | 3987324 | C | T | intron_variant | MODIFIER | c.1221+76C>T| |
S142 |
7 | BAA10g07160 | A10 | 3987417 | G | A | intron_variant | MODIFIER | c.1222-42G>A| |
S236 |
8 | BAA10g07160 | A10 | 3987919 | C | T | intron_variant | MODIFIER | c.1624+58C>T| |
S135 |
9 | BAA10g07160 | A10 | 3988512 | G | A | intron_variant | MODIFIER | c.1624+651G>A| |
S245 |
10 | BAA10g07160 | A10 | 3988536 | G | A | intron_variant | MODIFIER | c.1624+675G>A| |
S262 |
11 | BAA10g07160 | A10 | 3988575 | C | T | intron_variant | MODIFIER | c.1624+714C>T| |
S19 |
12 | BAA10g07160 | A10 | 3988798 | G | A | intron_variant | MODIFIER | c.1625-831G>A| |
S55 |
13 | BAA10g07160 | A10 | 3989591 | C | T | intron_variant | MODIFIER | c.1625-38C>T| |
S246 |
14 | BAA10g07160 | A10 | 3990612 | G | A | missense_variant | MODERATE | c.2245G>A|p.Gly749Arg |
S202 |
15 | BAA10g07160 | A10 | 3991026 | G | A | missense_variant | MODERATE | c.2572G>A|p.Val858Met |
S236 |
16 | BAA10g07160 | A10 | 3991472 | C | T | intron_variant | MODIFIER | c.2695+323C>T| |
S199 |
17 | BAA10g07160 | A10 | 3991843 | C | T | intron_variant | MODIFIER | c.2696-496C>T| |
S243 S299 |
18 | BAA10g07160 | A10 | 3992172 | G | A | intron_variant | MODIFIER | c.2696-167G>A| |
S208 S219 |
19 | BAA10g07160 | A10 | 3993312 | C | G | downstream_gene_variant | MODIFIER | c.*500C>G| |
S109 |
20 | BAA10g07160 | A10 | 3993575 | C | T | downstream_gene_variant | MODIFIER | c.*763C>T| |
S199 |
21 | BAA10g07160 | A10 | 3993846 | C | T | downstream_gene_variant | MODIFIER | c.*1034C>T| |
S271 |
22 | BAA10g07160 | A10 | 3994757 | C | T | downstream_gene_variant | MODIFIER | c.*1945C>T| |
S117 |
23 | BAA10g07160 | A10 | 3995993 | G | A | downstream_gene_variant | MODIFIER | c.*3181G>A| |
S178 |
24 | BAA10g07160 | A10 | 3996589 | G | A | downstream_gene_variant | MODIFIER | c.*3777G>A| |
S4 |
25 | BAA10g07160 | A10 | 3997690 | C | T | downstream_gene_variant | MODIFIER | c.*4878C>T| |
S11 S189 |