Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g18640 | A08 | 14880574 | C | T | upstream_gene_variant | MODIFIER | c.-4155C>T| |
S158 |
2 | BAA08g18640 | A08 | 14881048 | G | A | upstream_gene_variant | MODIFIER | c.-3681G>A| |
S66 |
3 | BAA08g18640 | A08 | 14881473 | G | A | upstream_gene_variant | MODIFIER | c.-3256G>A| |
S16 |
4 | BAA08g18640 | A08 | 14882557 | G | A | upstream_gene_variant | MODIFIER | c.-2172G>A| |
S219 S72 |
5 | BAA08g18640 | A08 | 14883360 | G | A | upstream_gene_variant | MODIFIER | c.-1369G>A| |
S107 |
6 | BAA08g18640 | A08 | 14883543 | G | A | upstream_gene_variant | MODIFIER | c.-1186G>A| |
S72 S78 |
7 | BAA08g18640 | A08 | 14883581 | G | A | upstream_gene_variant | MODIFIER | c.-1148G>A| |
S275 |
8 | BAA08g18640 | A08 | 14884828 | G | A | missense_variant | MODERATE | c.100G>A|p.Asp34Asn |
S274 |
9 | BAA08g18640 | A08 | 14885142 | G | A | intron_variant | MODIFIER | c.394-19G>A| |
S275 |
10 | BAA08g18640 | A08 | 14886371 | G | A | missense_variant | MODERATE | c.926G>A|p.Arg309Lys |
S66 |
11 | BAA08g18640 | A08 | 14886469 | C | T | intron_variant | MODIFIER | c.967-39C>T| |
S143 |
12 | BAA08g18640 | A08 | 14886489 | C | T | intron_variant | MODIFIER | c.967-19C>T| |
S284 |
13 | BAA08g18640 | A08 | 14886704 | G | A | missense_variant | MODERATE | c.1163G>A|p.Gly388Asp |
S266 |
14 | BAA08g18640 | A08 | 14887038 | G | A | intron_variant | MODIFIER | c.1298+199G>A| |
S221 |
15 | BAA08g18640 | A08 | 14887763 | C | T | intron_variant | MODIFIER | c.1359+132C>T| |
S251 |
16 | BAA08g18640 | A08 | 14888189 | C | T | intron_variant | MODIFIER | c.1359+558C>T| |
S268 |
17 | BAA08g18640 | A08 | 14888601 | C | T | intron_variant | MODIFIER | c.1360-657C>T| |
S293 |
18 | BAA08g18640 | A08 | 14888868 | G | A | intron_variant | MODIFIER | c.1360-390G>A| |
S32 |
19 | BAA08g18640 | A08 | 14889555 | G | A | intron_variant | MODIFIER | c.1542+115G>A| |
S279 |
20 | BAA08g18640 | A08 | 14889852 | G | A | missense_variant | MODERATE | c.1579G>A|p.Glu527Lys |
S292 |
21 | BAA08g18640 | A08 | 14889939 | C | T | missense_variant | MODERATE | c.1666C>T|p.His556Tyr |
S183 S198 |
22 | BAA08g18640 | A08 | 14890629 | C | T | downstream_gene_variant | MODIFIER | c.*679C>T| |
S251 |
23 | BAA08g18640 | A08 | 14891239 | G | A | downstream_gene_variant | MODIFIER | c.*1289G>A| |
S8 |
24 | BAA08g18640 | A08 | 14891479 | G | A | downstream_gene_variant | MODIFIER | c.*1529G>A| |
S205 |
25 | BAA08g18640 | A08 | 14892103 | G | A | downstream_gene_variant | MODIFIER | c.*2153G>A| |
S30 |