| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g17650 | A07 | 23914838 | G | A | upstream_gene_variant | MODIFIER | c.-71G>A| |
S239 |
| 2 | BAA07g17650 | A07 | 23915363 | G | A | intron_variant | MODIFIER | c.138+212G>A| |
S132 S137 S215 S89 |
| 3 | BAA07g17650 | A07 | 23915937 | C | T | missense_variant | MODERATE | c.467C>T|p.Thr156Ile |
S60 |
| 4 | BAA07g17650 | A07 | 23915978 | G | A | splice_region_variant&intron_variant | LOW | c.505+3G>A| |
S200 |
| 5 | BAA07g17650 | A07 | 23916188 | G | A | intron_variant | MODIFIER | c.505+213G>A| |
S143 |
| 6 | BAA07g17650 | A07 | 23916767 | C | T | synonymous_variant | LOW | c.588C>T|p.Thr196Thr |
S256 |
| 7 | BAA07g17650 | A07 | 23916786 | G | A | missense_variant | MODERATE | c.607G>A|p.Asp203Asn |
S120 |
| 8 | BAA07g17650 | A07 | 23916917 | C | T | intron_variant | MODIFIER | c.687+51C>T| |
S47 |
| 9 | BAA07g17650 | A07 | 23917391 | C | A | synonymous_variant | LOW | c.867C>A|p.Thr289Thr |
S115 |
| 10 | BAA07g17650 | A07 | 23918694 | G | A | intron_variant | MODIFIER | c.1273-114G>A| |
S46 |
| 11 | BAA07g17650 | A07 | 23918971 | C | T | missense_variant | MODERATE | c.1436C>T|p.Ser479Phe |
S56 |
| 12 | BAA07g17650 | A07 | 23919235 | C | T | intron_variant | MODIFIER | c.1585+115C>T| |
S274 |
| 13 | BAA07g17650 | A07 | 23919383 | G | A | intron_variant | MODIFIER | c.1585+263G>A| |
S31 |
| 14 | BAA07g17650 | A07 | 23919727 | G | A | intron_variant | MODIFIER | c.1585+607G>A| |
S115 |
| 15 | BAA07g17650 | A07 | 23920477 | C | T | synonymous_variant | LOW | c.1596C>T|p.Arg532Arg |
S59 |
| 16 | BAA07g17650 | A07 | 23920527 | C | T | missense_variant | MODERATE | c.1646C>T|p.Ser549Phe |
S155 S211 |
| 17 | BAA07g17650 | A07 | 23920598 | G | A | missense_variant | MODERATE | c.1717G>A|p.Gly573Arg |
S208 S219 |
| 18 | BAA07g17650 | A07 | 23920710 | C | T | missense_variant | MODERATE | c.1829C>T|p.Ala610Val |
S155 S211 |
| 19 | BAA07g17650 | A07 | 23920828 | C | T | synonymous_variant | LOW | c.1947C>T|p.Pro649Pro |
S191 |
| 20 | BAA07g17650 | A07 | 23920932 | C | T | splice_region_variant&intron_variant | LOW | c.1985-4C>T| |
S149 |
| 21 | BAA07g17650 | A07 | 23920997 | C | T | synonymous_variant | LOW | c.2046C>T|p.Leu682Leu |
S265 |
| 22 | BAA07g17650 | A07 | 23921425 | G | A | missense_variant | MODERATE | c.2068G>A|p.Glu690Lys |
S28 |
| 23 | BAA07g17650 | A07 | 23921940 | G | A | missense_variant | MODERATE | c.2371G>A|p.Asp791Asn |
S46 |
| 24 | BAA07g17650 | A07 | 23923178 | C | T | missense_variant | MODERATE | c.3053C>T|p.Ser1018Phe |
S16 |