| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g20190 | A03 | 9012883 | G | A | upstream_gene_variant | MODIFIER | c.-4140G>A| |
S269 |
| 2 | BAA03g20190 | A03 | 9013199 | C | T | upstream_gene_variant | MODIFIER | c.-3824C>T| |
S8 |
| 3 | BAA03g20190 | A03 | 9017197 | G | A | missense_variant | MODERATE | c.175G>A|p.Gly59Ser |
S210 S225 |
| 4 | BAA03g20190 | A03 | 9017606 | C | T | intron_variant | MODIFIER | c.478+30C>T| |
S293 |
| 5 | BAA03g20190 | A03 | 9017645 | C | T | intron_variant | MODIFIER | c.479-16C>T| |
S277 |
| 6 | BAA03g20190 | A03 | 9017777 | G | A | missense_variant | MODERATE | c.595G>A|p.Asp199Asn |
S109 |
| 7 | BAA03g20190 | A03 | 9018560 | G | A | intron_variant | MODIFIER | c.1116-25G>A| |
S125 |
| 8 | BAA03g20190 | A03 | 9018648 | G | A | synonymous_variant | LOW | c.1179G>A|p.Lys393Lys |
S282 |
| 9 | BAA03g20190 | A03 | 9018667 | C | T | missense_variant | MODERATE | c.1198C>T|p.His400Tyr |
S74 |
| 10 | BAA03g20190 | A03 | 9018835 | G | A | missense_variant | MODERATE | c.1366G>A|p.Gly456Arg |
S95 |
| 11 | BAA03g20190 | A03 | 9018939 | C | T | intron_variant | MODIFIER | c.1432+38C>T| |
S292 |
| 12 | BAA03g20190 | A03 | 9019779 | G | A | missense_variant | MODERATE | c.1945G>A|p.Glu649Lys |
S262 |
| 13 | BAA03g20190 | A03 | 9020088 | C | T | synonymous_variant | LOW | c.2181C>T|p.His727His |
S87 |
| 14 | BAA03g20190 | A03 | 9020304 | C | T | synonymous_variant | LOW | c.2397C>T|p.Leu799Leu |
S17 |
| 15 | BAA03g20190 | A03 | 9021160 | C | T | missense_variant | MODERATE | c.2849C>T|p.Ala950Val |
S139 |
| 16 | BAA03g20190 | A03 | 9021341 | C | T | synonymous_variant | LOW | c.3030C>T|p.Ser1010Ser |
S155 |
| 17 | BAA03g20190 | A03 | 9021683 | G | A | synonymous_variant | LOW | c.3372G>A|p.Leu1124Leu |
S269 |
| 18 | BAA03g20190 | A03 | 9021699 | G | A | missense_variant | MODERATE | c.3388G>A|p.Glu1130Lys |
S289 S290 |
| 19 | BAA03g20190 | A03 | 9022317 | G | A | missense_variant | MODERATE | c.4006G>A|p.Asp1336Asn |
S296 |