| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g29740 | A09 | 20605973 | C | T | downstream_gene_variant | MODIFIER | c.*3076G>A| |
S151 S263 |
| 2 | BAA09g29740 | A09 | 20607682 | C | T | downstream_gene_variant | MODIFIER | c.*1367G>A| |
S168 |
| 3 | BAA09g29740 | A09 | 20607960 | C | T | downstream_gene_variant | MODIFIER | c.*1089G>A| |
S168 |
| 4 | BAA09g29740 | A09 | 20608637 | C | T | downstream_gene_variant | MODIFIER | c.*412G>A| |
S219 S72 |
| 5 | BAA09g29740 | A09 | 20609084 | C | T | missense_variant | MODERATE | c.1735G>A|p.Asp579Asn |
S284 |
| 6 | BAA09g29740 | A09 | 20610752 | C | T | synonymous_variant | LOW | c.942G>A|p.Val314Val |
S87 |
| 7 | BAA09g29740 | A09 | 20610756 | G | A | missense_variant | MODERATE | c.938C>T|p.Ser313Phe |
S160 |
| 8 | BAA09g29740 | A09 | 20610976 | G | A | missense_variant | MODERATE | c.803C>T|p.Thr268Ile |
S288 |
| 9 | BAA09g29740 | A09 | 20610996 | C | T | synonymous_variant | LOW | c.783G>A|p.Glu261Glu |
S234 |
| 10 | BAA09g29740 | A09 | 20611735 | C | T | intron_variant | MODIFIER | c.750-706G>A| |
S293 |
| 11 | BAA09g29740 | A09 | 20612527 | C | T | intron_variant | MODIFIER | c.750-1498G>A| |
S256 |
| 12 | BAA09g29740 | A09 | 20612542 | G | A | intron_variant | MODIFIER | c.750-1513C>T| |
S240 |
| 13 | BAA09g29740 | A09 | 20612846 | C | T | intron_variant | MODIFIER | c.750-1817G>A| |
S115 |
| 14 | BAA09g29740 | A09 | 20614190 | C | T | intron_variant | MODIFIER | c.750-3161G>A| |
S269 |
| 15 | BAA09g29740 | A09 | 20614842 | G | A | intron_variant | MODIFIER | c.749+3418C>T| |
S244 |
| 16 | BAA09g29740 | A09 | 20615649 | C | T | intron_variant | MODIFIER | c.749+2611G>A| |
S188 |
| 17 | BAA09g29740 | A09 | 20615808 | G | A | intron_variant | MODIFIER | c.749+2452C>T| |
S16 |
| 18 | BAA09g29740 | A09 | 20615813 | G | A | intron_variant | MODIFIER | c.749+2447C>T| |
S16 |
| 19 | BAA09g29740 | A09 | 20615926 | G | A | intron_variant | MODIFIER | c.749+2334C>T| |
S251 |
| 20 | BAA09g29740 | A09 | 20616801 | C | T | intron_variant | MODIFIER | c.749+1459G>A| |
S136 |
| 21 | BAA09g29740 | A09 | 20616806 | G | A | intron_variant | MODIFIER | c.749+1454C>T| |
S135 S152 S273 S68 |
| 22 | BAA09g29740 | A09 | 20616924 | C | T | intron_variant | MODIFIER | c.749+1336G>A| |
S9 |
| 23 | BAA09g29740 | A09 | 20616969 | C | T | intron_variant | MODIFIER | c.749+1291G>A| |
S54 |
| 24 | BAA09g29740 | A09 | 20619328 | G | A | splice_region_variant&synonymous_variant | LOW | c.210C>T|p.Val70Val |
S181 |
| 25 | BAA09g29740 | A09 | 20620402 | G | A | upstream_gene_variant | MODIFIER | c.-630C>T| |
S165 |