Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11760 | A01 | 5473740 | G | A | intron_variant | MODIFIER | c.337-23C>T| |
S183 S198 |
2 | BAA01g11760 | A01 | 5473843 | G | A | intron_variant | MODIFIER | c.336+41C>T| |
S121 |
3 | BAA01g11760 | A01 | 5474496 | G | A | missense_variant | MODERATE | c.10C>T|p.Pro4Ser |
S154 S95 |
4 | BAA01g11760 | A01 | 5474519 | G | A | upstream_gene_variant | MODIFIER | c.-14C>T| |
S72 |
5 | BAA01g11760 | A01 | 5474657 | C | T | upstream_gene_variant | MODIFIER | c.-152G>A| |
S266 |
6 | BAA01g11760 | A01 | 5474667 | G | A | upstream_gene_variant | MODIFIER | c.-162C>T| |
S86 |
7 | BAA01g11760 | A01 | 5475104 | C | T | upstream_gene_variant | MODIFIER | c.-599G>A| |
S244 |
8 | BAA01g11760 | A01 | 5475766 | G | T | upstream_gene_variant | MODIFIER | c.-1261C>A| |
S268 |
9 | BAA01g11760 | A01 | 5475783 | C | T | upstream_gene_variant | MODIFIER | c.-1278G>A| |
S40 S49 |
10 | BAA01g11760 | A01 | 5477127 | G | A | upstream_gene_variant | MODIFIER | c.-2622C>T| |
S199 |
11 | BAA01g11760 | A01 | 5477206 | C | T | upstream_gene_variant | MODIFIER | c.-2701G>A| |
S48 |
12 | BAA01g11760 | A01 | 5477359 | G | A | upstream_gene_variant | MODIFIER | c.-2854C>T| |
S45 |
13 | BAA01g11760 | A01 | 5477547 | G | A | upstream_gene_variant | MODIFIER | c.-3042C>T| |
S70 |
14 | BAA01g11760 | A01 | 5477572 | G | A | upstream_gene_variant | MODIFIER | c.-3067C>T| |
S187 |
15 | BAA01g11760 | A01 | 5477787 | C | T | upstream_gene_variant | MODIFIER | c.-3282G>A| |
S6 |
16 | BAA01g11760 | A01 | 5479069 | G | A | upstream_gene_variant | MODIFIER | c.-4564C>T| |
S59 |