Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05830 | A08 | 4499465 | C | T | upstream_gene_variant | MODIFIER | c.-4713C>T| |
S47 |
2 | BAA08g05830 | A08 | 4500928 | G | A | upstream_gene_variant | MODIFIER | c.-3250G>A| |
S190 |
3 | BAA08g05830 | A08 | 4503539 | G | A | upstream_gene_variant | MODIFIER | c.-639G>A| |
S38 |
4 | BAA08g05830 | A08 | 4504415 | C | T | missense_variant | MODERATE | c.67C>T|p.Arg23Cys |
S63 |
5 | BAA08g05830 | A08 | 4504519 | C | T | synonymous_variant | LOW | c.171C>T|p.Arg57Arg |
S162 |
6 | BAA08g05830 | A08 | 4504606 | G | A | synonymous_variant | LOW | c.258G>A|p.Pro86Pro |
S193 |
7 | BAA08g05830 | A08 | 4505609 | C | T | missense_variant | MODERATE | c.716C>T|p.Ser239Phe |
S66 |
8 | BAA08g05830 | A08 | 4507376 | C | T | intron_variant | MODIFIER | c.1906-78C>T| |
S276 |
9 | BAA08g05830 | A08 | 4509306 | G | A | intron_variant | MODIFIER | c.1999+1759G>A| |
S5 |
10 | BAA08g05830 | A08 | 4509778 | G | A | intron_variant | MODIFIER | c.1999+2231G>A| |
S262 |
11 | BAA08g05830 | A08 | 4509830 | C | T | intron_variant | MODIFIER | c.1999+2283C>T| |
S206 S26 |
12 | BAA08g05830 | A08 | 4509968 | C | T | intron_variant | MODIFIER | c.1999+2421C>T| |
S206 S26 |
13 | BAA08g05830 | A08 | 4510050 | G | A | intron_variant | MODIFIER | c.1999+2503G>A| |
S139 |
14 | BAA08g05830 | A08 | 4510503 | G | A | intron_variant | MODIFIER | c.1999+2956G>A| |
S301 S304 |
15 | BAA08g05830 | A08 | 4512290 | C | T | intron_variant | MODIFIER | c.1999+4743C>T| |
S131 |
16 | BAA08g05830 | A08 | 4512436 | G | A | intron_variant | MODIFIER | c.1999+4889G>A| |
S194 |
17 | BAA08g05830 | A08 | 4513526 | G | A | intron_variant | MODIFIER | c.2000-5257G>A| |
S94 |
18 | BAA08g05830 | A08 | 4513919 | G | A | intron_variant | MODIFIER | c.2000-4864G>A| |
S16 |
19 | BAA08g05830 | A08 | 4514723 | C | T | intron_variant | MODIFIER | c.2000-4060C>T| |
S1 S90 |
20 | BAA08g05830 | A08 | 4514868 | C | T | intron_variant | MODIFIER | c.2000-3915C>T| |
S57 |
21 | BAA08g05830 | A08 | 4515578 | C | T | intron_variant | MODIFIER | c.2000-3205C>T| |
S183 S198 |
22 | BAA08g05830 | A08 | 4516635 | G | A | intron_variant | MODIFIER | c.2000-2148G>A| |
S188 S243 S299 |
23 | BAA08g05830 | A08 | 4516772 | G | A | intron_variant | MODIFIER | c.2000-2011G>A| |
S96 |
24 | BAA08g05830 | A08 | 4518183 | G | A | intron_variant | MODIFIER | c.2000-600G>A| |
S240 |
25 | BAA08g05830 | A08 | 4518837 | G | A | missense_variant | MODERATE | c.2054G>A|p.Arg685Gln |
S94 |