| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g06070 | A01 | 2721523 | G | A | missense_variant | MODERATE | c.148G>A|p.Glu50Lys |
S281 |
| 2 | BAA01g06070 | A01 | 2721738 | C | T | missense_variant | MODERATE | c.283C>T|p.Pro95Ser |
S38 |
| 3 | BAA01g06070 | A01 | 2721853 | C | T | missense_variant | MODERATE | c.398C>T|p.Ser133Phe |
S129 |
| 4 | BAA01g06070 | A01 | 2721879 | C | T | missense_variant | MODERATE | c.424C>T|p.Leu142Phe |
S242 |
| 5 | BAA01g06070 | A01 | 2722136 | C | T | synonymous_variant | LOW | c.525C>T|p.Ala175Ala |
S155 S211 |
| 6 | BAA01g06070 | A01 | 2722730 | C | T | missense_variant | MODERATE | c.944C>T|p.Ser315Phe |
S148 S210 S30 S31 |
| 7 | BAA01g06070 | A01 | 2722994 | C | T | missense_variant | MODERATE | c.1094C>T|p.Pro365Leu |
S69 |
| 8 | BAA01g06070 | A01 | 2723174 | G | A | missense_variant | MODERATE | c.1274G>A|p.Arg425Lys |
S279 |
| 9 | BAA01g06070 | A01 | 2723378 | G | A | synonymous_variant | LOW | c.1386G>A|p.Val462Val |
S289 S290 |
| 10 | BAA01g06070 | A01 | 2723836 | C | T | splice_region_variant&synonymous_variant | LOW | c.1629C>T|p.Ile543Ile |
S223 |
| 11 | BAA01g06070 | A01 | 2723953 | C | T | synonymous_variant | LOW | c.1746C>T|p.Tyr582Tyr |
S170 |
| 12 | BAA01g06070 | A01 | 2724584 | C | T | missense_variant | MODERATE | c.2192C>T|p.Thr731Met |
S48 |
| 13 | BAA01g06070 | A01 | 2724940 | G | A | missense_variant | MODERATE | c.2470G>A|p.Gly824Arg |
S279 |
| 14 | BAA01g06070 | A01 | 2725103 | C | T | missense_variant | MODERATE | c.2633C>T|p.Thr878Ile |
S252 |
| 15 | BAA01g06070 | A01 | 2725221 | G | A | missense_variant | MODERATE | c.2660G>A|p.Ser887Asn |
S172 S217 |
| 16 | BAA01g06070 | A01 | 2725794 | G | A | missense_variant | MODERATE | c.3233G>A|p.Gly1078Asp |
S107 |
| 17 | BAA01g06070 | A01 | 2726056 | C | T | downstream_gene_variant | MODIFIER | c.*252C>T| |
S76 |
| 18 | BAA01g06070 | A01 | 2726213 | C | T | downstream_gene_variant | MODIFIER | c.*409C>T| |
S170 |
| 19 | BAA01g06070 | A01 | 2726877 | C | T | downstream_gene_variant | MODIFIER | c.*1073C>T| |
S50 |