| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 20351 | BAA01g15050 | A01 | 7178138 | C | T | missense_variant | MODERATE | c.775C>T|p.Pro259Ser |
S108 |
| 20352 | BAA01g15050 | A01 | 7178285 | G | A | splice_region_variant&intron_variant | LOW | c.818-4G>A| |
S296 |
| 20353 | BAA01g15050 | A01 | 7178288 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.818-1G>A| |
S115 |
| 20354 | BAA01g15040 | A01 | 7179168 | C | T | upstream_gene_variant | MODIFIER | c.-3377G>A| |
S198 |
| 20355 | BAA01g15080 | A01 | 7181320 | G | A | upstream_gene_variant | MODIFIER | c.-4604G>A| |
S171 |
| 20356 | BAA01g15060 | A01 | 7182709 | C | T | splice_donor_variant&intron_variant | HIGH | c.261+1G>A| |
S71 |
| 20357 | BAA01g15060 | A01 | 7183641 | C | T | upstream_gene_variant | MODIFIER | c.-671G>A| |
S233 |
| 20358 | BAA01g15070 | A01 | 7183803 | T | G | synonymous_variant | LOW | c.192A>C|p.Ala64Ala |
S137 |
| 20359 | BAA01g15060 | A01 | 7184374 | C | T | upstream_gene_variant | MODIFIER | c.-1404G>A| |
S302 |
| 20360 | BAA01g15080 | A01 | 7186194 | C | T | missense_variant | MODERATE | c.271C>T|p.Leu91Phe |
S179 |
| 20361 | BAA01g15080 | A01 | 7186569 | C | T | synonymous_variant | LOW | c.646C>T|p.Leu216Leu |
S67 |
| 20362 | BAA01g15080 | A01 | 7189762 | G | A | missense_variant | MODERATE | c.1469G>A|p.Arg490Lys |
S217 S248 |
| 20363 | BAA01g15080 | A01 | 7190892 | C | T | intron_variant | MODIFIER | c.2153+33C>T| |
S9 |
| 20364 | BAA01g15090 | A01 | 7191184 | G | A | upstream_gene_variant | MODIFIER | c.-4933G>A| |
S175 |
| 20365 | BAA01g15090 | A01 | 7191254 | C | T | upstream_gene_variant | MODIFIER | c.-4863C>T| |
S112 |
| 20366 | BAA01g15090 | A01 | 7191738 | C | T | upstream_gene_variant | MODIFIER | c.-4379C>T| |
S11 |
| 20367 | BAA01g15090 | A01 | 7192218 | G | A | upstream_gene_variant | MODIFIER | c.-3899G>A| |
S37 |
| 20368 | BAA01g15080 | A01 | 7192951 | C | T | synonymous_variant | LOW | c.2295C>T|p.Thr765Thr |
S296 |
| 20369 | BAA01g15080 | A01 | 7192970 | G | A | missense_variant | MODERATE | c.2314G>A|p.Ala772Thr |
S237 |
| 20370 | BAA01g15090 | A01 | 7194934 | G | A | upstream_gene_variant | MODIFIER | c.-1183G>A| |
S168 |
| 20371 | BAA01g15090 | A01 | 7194946 | G | A | upstream_gene_variant | MODIFIER | c.-1171G>A| |
S287 |
| 20372 | BAA01g15090 | A01 | 7195215 | G | A | upstream_gene_variant | MODIFIER | c.-902G>A| |
S294 |
| 20373 | BAA01g15090 | A01 | 7195437 | G | A | upstream_gene_variant | MODIFIER | c.-680G>A| |
S195 |
| 20374 | BAA01g15090 | A01 | 7196389 | G | A | missense_variant | MODERATE | c.182G>A|p.Arg61His |
S97 |
| 20375 | BAA01g15090 | A01 | 7196403 | G | A | missense_variant | MODERATE | c.196G>A|p.Glu66Lys |
S104 S52 |