| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 56751 | BAA01g30790 | A01 | 19735341 | A | C | missense_variant | MODERATE | c.1262T>G|p.Leu421Arg |
S109 S37 S89 |
| 56752 | BAA01g30790 | A01 | 19736140 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.931-1G>A| |
S39 |
| 56753 | BAA01g30790 | A01 | 19736663 | G | A | intron_variant | MODIFIER | c.637-158C>T| |
S286 |
| 56754 | BAA01g30790 | A01 | 19738611 | C | T | missense_variant&splice_region_variant | MODERATE | c.253G>A|p.Gly85Arg |
S134 |
| 56755 | BAA01g30790 | A01 | 19739610 | G | A | upstream_gene_variant | MODIFIER | c.-747C>T| |
S294 |
| 56756 | BAA01g30790 | A01 | 19739648 | C | T | upstream_gene_variant | MODIFIER | c.-785G>A| |
S69 |
| 56757 | BAA01g30790 | A01 | 19740496 | C | T | upstream_gene_variant | MODIFIER | c.-1633G>A| |
S139 |
| 56758 | BAA01g30790 | A01 | 19740524 | C | T | upstream_gene_variant | MODIFIER | c.-1661G>A| |
S158 |
| 56759 | BAA01g30790 | A01 | 19741085 | C | T | upstream_gene_variant | MODIFIER | c.-2222G>A| |
S47 |
| 56760 | BAA01g30790 | A01 | 19741137 | C | T | upstream_gene_variant | MODIFIER | c.-2274G>A| |
S289 S290 |
| 56761 | BAA01g30790 | A01 | 19742684 | C | T | upstream_gene_variant | MODIFIER | c.-3821G>A| |
S162 |
| 56762 | BAA01g30790 | A01 | 19742860 | C | T | upstream_gene_variant | MODIFIER | c.-3997G>A| |
S4 |
| 56763 | BAA01g30800 | A01 | 19743033 | C | T | synonymous_variant | LOW | c.3459G>A|p.Lys1153Lys |
S185 |
| 56764 | BAA01g30800 | A01 | 19743462 | C | T | missense_variant | MODERATE | c.3220G>A|p.Asp1074Asn |
S275 |
| 56765 | BAA01g30800 | A01 | 19743526 | C | T | synonymous_variant | LOW | c.3156G>A|p.Ser1052Ser |
S294 |
| 56766 | BAA01g30800 | A01 | 19743577 | G | A | synonymous_variant | LOW | c.3105C>T|p.Phe1035Phe |
S298 |
| 56767 | BAA01g30800 | A01 | 19743776 | G | A | missense_variant | MODERATE | c.2906C>T|p.Ser969Leu |
S196 |
| 56768 | BAA01g30800 | A01 | 19744048 | G | A | intron_variant | MODIFIER | c.2751+74C>T| |
S263 |
| 56769 | BAA01g30800 | A01 | 19744166 | C | T | missense_variant | MODERATE | c.2707G>A|p.Glu903Lys |
S303 |
| 56770 | BAA01g30800 | A01 | 19744301 | C | T | missense_variant | MODERATE | c.2572G>A|p.Ala858Thr |
S64 |
| 56771 | BAA01g30800 | A01 | 19744476 | G | A | missense_variant | MODERATE | c.2525C>T|p.Ser842Phe |
S294 |
| 56772 | BAA01g30800 | A01 | 19744507 | C | T | missense_variant | MODERATE | c.2494G>A|p.Glu832Lys |
S162 |
| 56773 | BAA01g30800 | A01 | 19744908 | C | T | synonymous_variant | LOW | c.2178G>A|p.Lys726Lys |
S54 |
| 56774 | BAA01g30800 | A01 | 19745036 | G | A | missense_variant | MODERATE | c.2050C>T|p.Pro684Ser |
S116 |
| 56775 | BAA01g30800 | A01 | 19745376 | C | T | synonymous_variant | LOW | c.1710G>A|p.Glu570Glu |
S233 |