Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g22290 | A09 | 13940695 | C | T | downstream_gene_variant | MODIFIER | c.*1829G>A| |
S256 |
2 | BAA09g22290 | A09 | 13940839 | C | T | downstream_gene_variant | MODIFIER | c.*1685G>A| |
S231 |
3 | BAA09g22290 | A09 | 13941025 | C | T | downstream_gene_variant | MODIFIER | c.*1499G>A| |
S256 |
4 | BAA09g22290 | A09 | 13941313 | G | A | downstream_gene_variant | MODIFIER | c.*1211C>T| |
S284 |
5 | BAA09g22290 | A09 | 13941919 | C | T | downstream_gene_variant | MODIFIER | c.*605G>A| |
S281 |
6 | BAA09g22290 | A09 | 13942864 | G | A | missense_variant | MODERATE | c.2156C>T|p.Ala719Val |
S233 |
7 | BAA09g22290 | A09 | 13942869 | C | T | stop_gained | HIGH | c.2151G>A|p.Trp717* |
S120 |
8 | BAA09g22290 | A09 | 13943435 | C | T | missense_variant | MODERATE | c.1585G>A|p.Asp529Asn |
S286 |
9 | BAA09g22290 | A09 | 13943887 | G | A | missense_variant | MODERATE | c.1316C>T|p.Ala439Val |
S20 |
10 | BAA09g22290 | A09 | 13944405 | C | T | synonymous_variant | LOW | c.798G>A|p.Lys266Lys |
S153 |
11 | BAA09g22290 | A09 | 13944513 | C | T | missense_variant | MODERATE | c.690G>A|p.Met230Ile |
S18 |
12 | BAA09g22290 | A09 | 13944572 | C | T | missense_variant | MODERATE | c.631G>A|p.Gly211Arg |
S278 |
13 | BAA09g22290 | A09 | 13944945 | G | A | splice_region_variant&intron_variant | LOW | c.393+7C>T| |
S12 |
14 | BAA09g22290 | A09 | 13944969 | C | T | missense_variant | MODERATE | c.376G>A|p.Asp126Asn |
S242 |
15 | BAA09g22290 | A09 | 13945334 | G | A | synonymous_variant | LOW | c.93C>T|p.Ser31Ser |
S89 |
16 | BAA09g22290 | A09 | 13945371 | C | T | missense_variant | MODERATE | c.56G>A|p.Gly19Asp |
S83 |
17 | BAA09g22290 | A09 | 13948207 | C | T | upstream_gene_variant | MODIFIER | c.-2781G>A| |
S204 |
18 | BAA09g22290 | A09 | 13950091 | C | T | upstream_gene_variant | MODIFIER | c.-4665G>A| |
S282 |