| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 198601 | BAA02g29810 | A02 | 17141703 | G | A | downstream_gene_variant | MODIFIER | c.*504C>T| |
S148 S30 S31 |
| 198602 | BAA02g29810 | A02 | 17141824 | C | T | downstream_gene_variant | MODIFIER | c.*383G>A| |
S224 |
| 198603 | BAA02g29810 | A02 | 17142292 | C | T | missense_variant | MODERATE | c.122G>A|p.Gly41Asp |
S73 S91 |
| 198604 | BAA02g29810 | A02 | 17142856 | G | A | upstream_gene_variant | MODIFIER | c.-443C>T| |
S113 |
| 198605 | BAA02g29820 | A02 | 17143521 | C | T | missense_variant | MODERATE | c.832G>A|p.Asp278Asn |
S124 |
| 198606 | BAA02g29820 | A02 | 17143974 | G | A | splice_region_variant&intron_variant | LOW | c.434+8C>T| |
S232 |
| 198607 | BAA02g29820 | A02 | 17144268 | C | T | missense_variant | MODERATE | c.148G>A|p.Asp50Asn |
S114 |
| 198608 | BAA02g29810 | A02 | 17144453 | C | T | upstream_gene_variant | MODIFIER | c.-2040G>A| |
S167 |
| 198609 | BAA02g29810 | A02 | 17145187 | C | T | upstream_gene_variant | MODIFIER | c.-2774G>A| |
S15 S156 S3 S34 |
| 198610 | BAA02g29810 | A02 | 17145514 | G | A | upstream_gene_variant | MODIFIER | c.-3101C>T| |
S281 |
| 198611 | BAA02g29810 | A02 | 17146101 | C | T | upstream_gene_variant | MODIFIER | c.-3688G>A| |
S167 |
| 198612 | BAA02g29810 | A02 | 17147238 | G | A | upstream_gene_variant | MODIFIER | c.-4825C>T| |
S265 |
| 198613 | BAA02g29820 | A02 | 17147522 | C | T | upstream_gene_variant | MODIFIER | c.-3107G>A| |
S152 |
| 198614 | BAA02g29820 | A02 | 17147737 | G | A | upstream_gene_variant | MODIFIER | c.-3322C>T| |
S10 |
| 198615 | BAA02g29830 | A02 | 17149844 | C | T | splice_region_variant&intron_variant | LOW | c.257-8G>A| |
S277 |
| 198616 | BAA02g29830 | A02 | 17150045 | G | A | synonymous_variant | LOW | c.69C>T|p.Ile23Ile |
S97 |
| 198617 | BAA02g29830 | A02 | 17150135 | C | T | upstream_gene_variant | MODIFIER | c.-22G>A| |
S216 |
| 198618 | BAA02g29840 | A02 | 17151426 | G | A | missense_variant | MODERATE | c.604C>T|p.Leu202Phe |
S143 |
| 198619 | BAA02g29830 | A02 | 17151541 | C | T | upstream_gene_variant | MODIFIER | c.-1428G>A| |
S202 |
| 198620 | BAA02g29840 | A02 | 17151925 | C | T | missense_variant | MODERATE | c.310G>A|p.Ala104Thr |
S305 |
| 198621 | BAA02g29830 | A02 | 17152703 | C | A | upstream_gene_variant | MODIFIER | c.-2590G>T| |
S274 |
| 198622 | BAA02g29830 | A02 | 17152802 | G | A | upstream_gene_variant | MODIFIER | c.-2689C>T| |
S125 |
| 198623 | BAA02g29830 | A02 | 17152929 | G | A | upstream_gene_variant | MODIFIER | c.-2816C>T| |
S35 |
| 198624 | BAA02g29850 | A02 | 17153354 | C | T | missense_variant | MODERATE | c.278C>T|p.Pro93Leu |
S287 |
| 198625 | BAA02g29850 | A02 | 17153463 | G | A | synonymous_variant | LOW | c.387G>A|p.Lys129Lys |
S72 S78 |