Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10050 | A10 | 11831416 | G | A | upstream_gene_variant | MODIFIER | c.-1363G>A| |
S306 S308 |
2 | BAA10g10050 | A10 | 11833795 | G | A | synonymous_variant | LOW | c.642G>A|p.Gln214Gln |
S139 |
3 | BAA10g10050 | A10 | 11835802 | G | A | missense_variant | MODERATE | c.1240G>A|p.Ala414Thr |
S245 |
4 | BAA10g10050 | A10 | 11836620 | C | T | intron_variant | MODIFIER | c.1600+240C>T| |
S308 |
5 | BAA10g10050 | A10 | 11837608 | G | A | intron_variant | MODIFIER | c.1872+161G>A| |
S148 S210 S30 S31 |
6 | BAA10g10050 | A10 | 11837870 | C | T | missense_variant | MODERATE | c.1900C>T|p.Leu634Phe |
S268 |
7 | BAA10g10050 | A10 | 11838363 | G | A | missense_variant | MODERATE | c.2125G>A|p.Ala709Thr |
S226 |
8 | BAA10g10050 | A10 | 11838872 | G | A | intron_variant | MODIFIER | c.2340+218G>A| |
S245 |
9 | BAA10g10050 | A10 | 11839976 | C | T | intron_variant | MODIFIER | c.2730-87C>T| |
S34 |
10 | BAA10g10050 | A10 | 11840435 | G | A | intron_variant | MODIFIER | c.2958+144G>A| |
S129 |
11 | BAA10g10050 | A10 | 11840526 | C | T | intron_variant | MODIFIER | c.2958+235C>T| |
S308 |
12 | BAA10g10050 | A10 | 11840599 | C | T | intron_variant | MODIFIER | c.2959-175C>T| |
S20 |
13 | BAA10g10050 | A10 | 11840946 | G | A | intron_variant | MODIFIER | c.3087+44G>A| |
S202 |
14 | BAA10g10050 | A10 | 11841173 | C | T | intron_variant | MODIFIER | c.3216+36C>T| |
S56 |
15 | BAA10g10050 | A10 | 11841309 | G | A | intron_variant | MODIFIER | c.3216+172G>A| |
S192 |
16 | BAA10g10050 | A10 | 11841533 | C | T | missense_variant | MODERATE | c.3224C>T|p.Ser1075Leu |
S103 |