| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 10651 | BAA01g08560 | A01 | 3798116 | G | A | intron_variant | MODIFIER | c.643-115G>A| |
S162 |
| 10652 | BAA01g08560 | A01 | 3798572 | G | A | synonymous_variant | LOW | c.810G>A|p.Glu270Glu |
S128 |
| 10653 | BAA01g08560 | A01 | 3798834 | C | T | intron_variant | MODIFIER | c.946-39C>T| |
S44 |
| 10654 | BAA01g08560 | A01 | 3799123 | C | T | intron_variant | MODIFIER | c.1021-42C>T| |
S18 |
| 10655 | BAA01g08560 | A01 | 3799730 | G | A | missense_variant | MODERATE | c.1327G>A|p.Gly443Arg |
S32 |
| 10656 | BAA01g08560 | A01 | 3800377 | C | T | missense_variant | MODERATE | c.1522C>T|p.Pro508Ser |
S4 |
| 10657 | BAA01g08580 | A01 | 3800640 | C | T | upstream_gene_variant | MODIFIER | c.-4992C>T| |
S53 |
| 10658 | BAA01g08580 | A01 | 3802788 | G | A | upstream_gene_variant | MODIFIER | c.-2844G>A| |
S247 |
| 10659 | BAA01g08560 | A01 | 3803016 | C | T | synonymous_variant | LOW | c.2826C>T|p.Leu942Leu |
S252 |
| 10660 | BAA01g08580 | A01 | 3804788 | C | T | upstream_gene_variant | MODIFIER | c.-844C>T| |
S167 |
| 10661 | BAA01g08570 | A01 | 3804977 | G | A | missense_variant | MODERATE | c.344C>T|p.Ser115Leu |
S113 |
| 10662 | BAA01g08570 | A01 | 3805080 | G | A | missense_variant | MODERATE | c.241C>T|p.Pro81Ser |
S116 |
| 10663 | BAA01g08570 | A01 | 3805210 | G | A | synonymous_variant | LOW | c.111C>T|p.Leu37Leu |
S105 S106 |
| 10664 | BAA01g08570 | A01 | 3805457 | G | A | upstream_gene_variant | MODIFIER | c.-137C>T| |
S289 S290 |
| 10665 | BAA01g08570 | A01 | 3805594 | G | A | upstream_gene_variant | MODIFIER | c.-274C>T| |
S83 |
| 10666 | BAA01g08570 | A01 | 3805774 | C | T | upstream_gene_variant | MODIFIER | c.-454G>A| |
S46 |
| 10667 | BAA01g08580 | A01 | 3806884 | C | T | synonymous_variant | LOW | c.606C>T|p.Ser202Ser |
S139 |
| 10668 | BAA01g08570 | A01 | 3807344 | G | A | upstream_gene_variant | MODIFIER | c.-2024C>T| |
S159 S243 |
| 10669 | BAA01g08580 | A01 | 3807957 | G | A | synonymous_variant | LOW | c.1068G>A|p.Val356Val |
S181 |
| 10670 | BAA01g08570 | A01 | 3808762 | C | T | upstream_gene_variant | MODIFIER | c.-3442G>A| |
S266 |
| 10671 | BAA01g08590 | A01 | 3809284 | C | T | missense_variant | MODERATE | c.263C>T|p.Ala88Val |
S40 S49 |
| 10672 | BAA01g08570 | A01 | 3809662 | G | A | upstream_gene_variant | MODIFIER | c.-4342C>T| |
S289 S290 |
| 10673 | BAA01g08600 | A01 | 3810251 | G | A | missense_variant | MODERATE | c.256G>A|p.Ala86Thr |
S187 |
| 10674 | BAA01g08600 | A01 | 3810382 | C | T | synonymous_variant | LOW | c.387C>T|p.Leu129Leu |
S295 |
| 10675 | BAA01g08600 | A01 | 3811413 | G | A | missense_variant | MODERATE | c.1418G>A|p.Gly473Glu |
S13 |