| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 26601 | BAA01g18950 | A01 | 9303526 | C | T | upstream_gene_variant | MODIFIER | c.-1826G>A| |
S242 |
| 26602 | BAA01g18950 | A01 | 9303556 | G | A | upstream_gene_variant | MODIFIER | c.-1856C>T| |
S178 |
| 26603 | BAA01g18950 | A01 | 9303560 | G | A | upstream_gene_variant | MODIFIER | c.-1860C>T| |
S209 |
| 26604 | BAA01g18960 | A01 | 9304304 | C | T | synonymous_variant | LOW | c.609G>A|p.Arg203Arg |
S113 |
| 26605 | BAA01g18960 | A01 | 9304897 | C | T | missense_variant | MODERATE | c.161G>A|p.Gly54Asp |
S20 |
| 26606 | BAA01g18960 | A01 | 9304932 | C | T | synonymous_variant | LOW | c.126G>A|p.Pro42Pro |
S36 |
| 26607 | BAA01g18960 | A01 | 9304934 | G | A | missense_variant | MODERATE | c.124C>T|p.Pro42Ser |
S201 |
| 26608 | BAA01g18960 | A01 | 9304940 | G | A | stop_gained | HIGH | c.118C>T|p.Gln40* |
S217 S248 |
| 26609 | BAA01g18970 | A01 | 9306432 | G | A | missense_variant | MODERATE | c.784G>A|p.Glu262Lys |
S180 |
| 26610 | BAA01g18970 | A01 | 9307260 | C | T | missense_variant | MODERATE | c.1535C>T|p.Ala512Val |
S286 |
| 26611 | BAA01g18970 | A01 | 9307277 | G | A | missense_variant | MODERATE | c.1552G>A|p.Ala518Thr |
S87 |
| 26612 | BAA01g18960 | A01 | 9307630 | G | A | upstream_gene_variant | MODIFIER | c.-2573C>T| |
S240 |
| 26613 | BAA01g18970 | A01 | 9308815 | G | A | missense_variant | MODERATE | c.2579G>A|p.Arg860Lys |
S13 |
| 26614 | BAA01g18970 | A01 | 9309369 | C | T | missense_variant | MODERATE | c.3133C>T|p.Pro1045Ser |
S179 |
| 26615 | BAA01g18970 | A01 | 9309854 | G | A | synonymous_variant | LOW | c.3618G>A|p.Lys1206Lys |
S225 S73 |
| 26616 | BAA01g18970 | A01 | 9310086 | C | T | synonymous_variant | LOW | c.3850C>T|p.Leu1284Leu |
S81 S85 |
| 26617 | BAA01g18970 | A01 | 9310777 | C | T | missense_variant | MODERATE | c.4541C>T|p.Ala1514Val |
S107 |
| 26618 | BAA01g18970 | A01 | 9310919 | C | T | synonymous_variant | LOW | c.4683C>T|p.Asp1561Asp |
S50 |
| 26619 | BAA01g18970 | A01 | 9311808 | C | T | missense_variant | MODERATE | c.5572C>T|p.Leu1858Phe |
S264 |
| 26620 | BAA01g18970 | A01 | 9312273 | G | A | splice_region_variant&intron_variant | LOW | c.5940+7G>A| |
S143 |
| 26621 | BAA01g18970 | A01 | 9312610 | G | A | missense_variant | MODERATE | c.6002G>A|p.Gly2001Glu |
S232 |
| 26622 | BAA01g18970 | A01 | 9312975 | C | T | missense_variant | MODERATE | c.6275C>T|p.Ser2092Phe |
S270 |
| 26623 | BAA01g18980 | A01 | 9317995 | G | A | upstream_gene_variant | MODIFIER | c.-344C>T| |
S235 |
| 26624 | BAA01g18990 | A01 | 9318280 | T | A | missense_variant | MODERATE | c.259T>A|p.Ser87Thr |
S279 |
| 26625 | BAA01g18980 | A01 | 9319931 | C | T | upstream_gene_variant | MODIFIER | c.-2280G>A| |
S158 |