Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g33760 | A03 | 15643717 | G | A | missense_variant | MODERATE | c.6206C>T|p.Thr2069Ile |
S78 S83 |
2 | BAA03g33760 | A03 | 15644099 | G | A | missense_variant | MODERATE | c.5824C>T|p.Pro1942Ser |
S89 |
3 | BAA03g33760 | A03 | 15644302 | C | T | missense_variant | MODERATE | c.5621G>A|p.Gly1874Glu |
S16 |
4 | BAA03g33760 | A03 | 15644410 | G | A | missense_variant | MODERATE | c.5513C>T|p.Pro1838Leu |
S169 |
5 | BAA03g33760 | A03 | 15644822 | G | A | missense_variant | MODERATE | c.5101C>T|p.Pro1701Ser |
S48 |
6 | BAA03g33760 | A03 | 15645170 | C | T | missense_variant | MODERATE | c.4753G>A|p.Ala1585Thr |
S208 |
7 | BAA03g33760 | A03 | 15645224 | G | A | missense_variant | MODERATE | c.4699C>T|p.Pro1567Ser |
S185 |
8 | BAA03g33760 | A03 | 15645286 | G | A | missense_variant | MODERATE | c.4637C>T|p.Ser1546Phe |
S32 |
9 | BAA03g33760 | A03 | 15645301 | C | T | missense_variant | MODERATE | c.4622G>A|p.Arg1541Gln |
S70 |
10 | BAA03g33760 | A03 | 15645744 | C | T | synonymous_variant | LOW | c.4266G>A|p.Ser1422Ser |
S98 |
11 | BAA03g33760 | A03 | 15645814 | G | A | missense_variant | MODERATE | c.4196C>T|p.Thr1399Ile |
S296 |
12 | BAA03g33760 | A03 | 15647721 | C | T | missense_variant | MODERATE | c.3229G>A|p.Glu1077Lys |
S125 |
13 | BAA03g33760 | A03 | 15648065 | G | A | intron_variant | MODIFIER | c.3123+11C>T| |
S305 |
14 | BAA03g33760 | A03 | 15648641 | G | A | synonymous_variant | LOW | c.2826C>T|p.Leu942Leu |
S12 |
15 | BAA03g33760 | A03 | 15648893 | G | A | intron_variant | MODIFIER | c.2704+49C>T| |
S175 |
16 | BAA03g33760 | A03 | 15649427 | G | A | missense_variant | MODERATE | c.2318C>T|p.Ala773Val |
S199 |
17 | BAA03g33760 | A03 | 15649859 | C | T | splice_region_variant&intron_variant | LOW | c.2055+5G>A| |
S40 S49 |
18 | BAA03g33760 | A03 | 15649878 | C | T | missense_variant | MODERATE | c.2041G>A|p.Gly681Ser |
S98 |
19 | BAA03g33760 | A03 | 15651124 | C | T | missense_variant | MODERATE | c.1334G>A|p.Ser445Asn |
S116 |
20 | BAA03g33760 | A03 | 15651836 | C | T | synonymous_variant | LOW | c.798G>A|p.Val266Val |
S113 |
21 | BAA03g33760 | A03 | 15652305 | C | T | missense_variant | MODERATE | c.329G>A|p.Arg110Gln |
S281 |
22 | BAA03g33760 | A03 | 15652657 | G | A | intron_variant | MODIFIER | c.288+152C>T| |
S303 |
23 | BAA03g33760 | A03 | 15652847 | G | A | missense_variant | MODERATE | c.250C>T|p.Leu84Phe |
S287 |
24 | BAA03g33760 | A03 | 15652964 | G | A | intron_variant | MODIFIER | c.165-32C>T| |
S186 |
25 | BAA03g33760 | A03 | 15653550 | G | A | intron_variant | MODIFIER | c.75+40C>T| |
S155 |