| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 21351 | BAA01g15560 | A01 | 7525270 | C | T | missense_variant | MODERATE | c.358G>A|p.Val120Met |
S294 |
| 21352 | BAA01g15550 | A01 | 7526157 | G | A | upstream_gene_variant | MODIFIER | c.-4451C>T| |
S191 |
| 21353 | BAA01g15560 | A01 | 7526940 | G | A | upstream_gene_variant | MODIFIER | c.-1313C>T| |
S70 |
| 21354 | BAA01g15560 | A01 | 7527693 | G | A | upstream_gene_variant | MODIFIER | c.-2066C>T| |
S181 |
| 21355 | BAA01g15560 | A01 | 7529721 | A | T | upstream_gene_variant | MODIFIER | c.-4094T>A| |
S118 |
| 21356 | BAA01g15560 | A01 | 7530018 | C | G | upstream_gene_variant | MODIFIER | c.-4391G>C| |
S244 |
| 21357 | BAA01g15560-BAA01g15570 | A01 | 7530778 | C | T | intergenic_region | MODIFIER | n.7530778C>T| |
S286 |
| 21358 | BAA01g15570 | A01 | 7534947 | G | A | downstream_gene_variant | MODIFIER | c.*2367C>T| |
S13 |
| 21359 | BAA01g15570 | A01 | 7535008 | C | T | downstream_gene_variant | MODIFIER | c.*2306G>A| |
S107 |
| 21360 | BAA01g15570 | A01 | 7539738 | C | T | upstream_gene_variant | MODIFIER | c.-922G>A| |
S230 |
| 21361 | BAA01g15570 | A01 | 7540171 | C | T | upstream_gene_variant | MODIFIER | c.-1355G>A| |
S42 |
| 21362 | BAA01g15570 | A01 | 7541063 | C | T | upstream_gene_variant | MODIFIER | c.-2247G>A| |
S81 S85 |
| 21363 | BAA01g15580 | A01 | 7542242 | C | T | missense_variant | MODERATE | c.2149G>A|p.Glu717Lys |
S177 |
| 21364 | BAA01g15580 | A01 | 7542832 | G | A | missense_variant | MODERATE | c.1559C>T|p.Ser520Phe |
S294 |
| 21365 | BAA01g15580 | A01 | 7542994 | G | A | missense_variant | MODERATE | c.1397C>T|p.Pro466Leu |
S202 |
| 21366 | BAA01g15580 | A01 | 7543896 | C | T | missense_variant | MODERATE | c.698G>A|p.Gly233Asp |
S184 |
| 21367 | BAA01g15580 | A01 | 7544010 | G | A | missense_variant | MODERATE | c.584C>T|p.Ser195Phe |
S180 |
| 21368 | BAA01g15580 | A01 | 7544179 | C | T | missense_variant | MODERATE | c.415G>A|p.Gly139Ser |
S113 |
| 21369 | BAA01g15580 | A01 | 7544206 | C | T | missense_variant | MODERATE | c.388G>A|p.Ala130Thr |
S226 |
| 21370 | BAA01g15580 | A01 | 7544273 | G | A | synonymous_variant | LOW | c.321C>T|p.Leu107Leu |
S280 |
| 21371 | BAA01g15580 | A01 | 7544459 | C | T | intron_variant | MODIFIER | c.193-58G>A| |
S185 |
| 21372 | BAA01g15580 | A01 | 7545056 | G | A | intron_variant | MODIFIER | c.192+10C>T| |
S45 |
| 21373 | BAA01g15580 | A01 | 7546786 | C | T | upstream_gene_variant | MODIFIER | c.-1529G>A| |
S100 |
| 21374 | BAA01g15580 | A01 | 7547699 | G | A | upstream_gene_variant | MODIFIER | c.-2442C>T| |
S70 |
| 21375 | BAA01g15590 | A01 | 7550344 | G | A | upstream_gene_variant | MODIFIER | c.-3221G>A| |
S5 |