| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 78751 | BAA01g41420 | A01 | 27534027 | C | T | missense_variant&splice_region_variant | MODERATE | c.844G>A|p.Glu282Lys |
S28 |
| 78752 | BAA01g41410 | A01 | 27534673 | C | T | upstream_gene_variant | MODIFIER | c.-3386G>A| |
S48 |
| 78753 | BAA01g41410 | A01 | 27534871 | G | A | upstream_gene_variant | MODIFIER | c.-3584C>T| |
S155 S211 |
| 78754 | BAA01g41420 | A01 | 27535491 | C | T | missense_variant | MODERATE | c.619G>A|p.Glu207Lys |
S132 S215 |
| 78755 | BAA01g41420 | A01 | 27537142 | G | A | upstream_gene_variant | MODIFIER | c.-1033C>T| |
S246 |
| 78756 | BAA01g41420 | A01 | 27537675 | G | A | upstream_gene_variant | MODIFIER | c.-1566C>T| |
S234 |
| 78757 | BAA01g41420 | A01 | 27537975 | C | T | upstream_gene_variant | MODIFIER | c.-1866G>A| |
S104 S52 |
| 78758 | BAA01g41430 | A01 | 27539160 | C | T | missense_variant&splice_region_variant | MODERATE | c.680C>T|p.Ala227Val |
S128 |
| 78759 | BAA01g41430 | A01 | 27539780 | G | A | splice_region_variant&intron_variant | LOW | c.1122+5G>A| |
S95 |
| 78760 | BAA01g41420 | A01 | 27540800 | C | T | upstream_gene_variant | MODIFIER | c.-4691G>A| |
S128 |
| 78761 | BAA01g41430 | A01 | 27541522 | C | T | intron_variant | MODIFIER | c.1713+53C>T| |
S264 |
| 78762 | BAA01g41440 | A01 | 27542260 | G | A | upstream_gene_variant | MODIFIER | c.-4909G>A| |
S204 |
| 78763 | BAA01g41430 | A01 | 27542627 | C | T | missense_variant | MODERATE | c.2104C>T|p.Pro702Ser |
S236 |
| 78764 | BAA01g41440 | A01 | 27544313 | C | T | upstream_gene_variant | MODIFIER | c.-2856C>T| |
S198 |
| 78765 | BAA01g41430 | A01 | 27544399 | G | A | synonymous_variant | LOW | c.2871G>A|p.Lys957Lys |
S138 |
| 78766 | BAA01g41440 | A01 | 27544734 | G | A | upstream_gene_variant | MODIFIER | c.-2435G>A| |
S163 |
| 78767 | BAA01g41440 | A01 | 27544789 | C | T | upstream_gene_variant | MODIFIER | c.-2380C>T| |
S53 |
| 78768 | BAA01g41430 | A01 | 27545143 | C | T | splice_region_variant&intron_variant | LOW | c.3030+5C>T| |
S7 |
| 78769 | BAA01g41430 | A01 | 27545329 | C | T | missense_variant | MODERATE | c.3118C>T|p.Leu1040Phe |
S228 |
| 78770 | BAA01g41440 | A01 | 27545379 | G | A | upstream_gene_variant | MODIFIER | c.-1790G>A| |
S103 |
| 78771 | BAA01g41430 | A01 | 27545509 | C | T | missense_variant | MODERATE | c.3178C>T|p.Pro1060Ser |
S8 |
| 78772 | BAA01g41440 | A01 | 27546447 | C | T | upstream_gene_variant | MODIFIER | c.-722C>T| |
S187 S243 S276 |
| 78773 | BAA01g41440 | A01 | 27547980 | C | T | missense_variant | MODERATE | c.812C>T|p.Ser271Phe |
S135 |
| 78774 | BAA01g41450 | A01 | 27548437 | C | T | upstream_gene_variant | MODIFIER | c.-4460C>T| |
S293 |
| 78775 | BAA01g41450 | A01 | 27549673 | G | A | upstream_gene_variant | MODIFIER | c.-3224G>A| |
S40 |