| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 34201 | BAA01g23070 | A01 | 11794106 | C | T | upstream_gene_variant | MODIFIER | c.-394G>A| |
S130 |
| 34202 | BAA01g23070 | A01 | 11794327 | T | G | upstream_gene_variant | MODIFIER | c.-615A>C| |
S11 S149 S205 S216 S257 S264 S280 S45 |
| 34203 | BAA01g23080 | A01 | 11794668 | G | A | synonymous_variant | LOW | c.36G>A|p.Thr12Thr |
S263 |
| 34204 | BAA01g23080 | A01 | 11795030 | G | A | missense_variant | MODERATE | c.239G>A|p.Gly80Asp |
S124 |
| 34205 | BAA01g23070 | A01 | 11795423 | G | A | upstream_gene_variant | MODIFIER | c.-1711C>T| |
S68 |
| 34206 | BAA01g23080 | A01 | 11796099 | C | T | missense_variant | MODERATE | c.799C>T|p.Pro267Ser |
S286 |
| 34207 | BAA01g23070 | A01 | 11796961 | G | A | upstream_gene_variant | MODIFIER | c.-3249C>T| |
S239 |
| 34208 | BAA01g23070 | A01 | 11798032 | G | A | upstream_gene_variant | MODIFIER | c.-4320C>T| |
S59 |
| 34209 | BAA01g23070 | A01 | 11798661 | C | T | upstream_gene_variant | MODIFIER | c.-4949G>A| |
S171 |
| 34210 | BAA01g23090 | A01 | 11798854 | C | T | upstream_gene_variant | MODIFIER | c.-1101G>A| |
S158 |
| 34211 | BAA01g23090 | A01 | 11802697 | G | A | upstream_gene_variant | MODIFIER | c.-4944C>T| |
S186 |
| 34212 | BAA01g23100 | A01 | 11803929 | C | T | upstream_gene_variant | MODIFIER | c.-1310C>T| |
S160 |
| 34213 | BAA01g23100 | A01 | 11804344 | C | T | upstream_gene_variant | MODIFIER | c.-895C>T| |
S143 |
| 34214 | BAA01g23100 | A01 | 11804360 | G | A | upstream_gene_variant | MODIFIER | c.-879G>A| |
S263 |
| 34215 | BAA01g23100 | A01 | 11804459 | C | T | upstream_gene_variant | MODIFIER | c.-780C>T| |
S198 |
| 34216 | BAA01g23100 | A01 | 11804676 | G | A | upstream_gene_variant | MODIFIER | c.-563G>A| |
S59 |
| 34217 | BAA01g23100 | A01 | 11805321 | C | T | intron_variant | MODIFIER | c.58+25C>T| |
S210 |
| 34218 | BAA01g23100 | A01 | 11806185 | C | T | intron_variant | MODIFIER | c.346+118C>T| |
S182 |
| 34219 | BAA01g23100 | A01 | 11806262 | C | T | intron_variant | MODIFIER | c.347-72C>T| |
S303 |
| 34220 | BAA01g23100 | A01 | 11806319 | G | A | intron_variant | MODIFIER | c.347-15G>A| |
S308 |
| 34221 | BAA01g23100 | A01 | 11806525 | C | T | missense_variant | MODERATE | c.538C>T|p.Pro180Ser |
S54 |
| 34222 | BAA01g23100 | A01 | 11806542 | G | A | synonymous_variant | LOW | c.555G>A|p.Glu185Glu |
S84 S93 |
| 34223 | BAA01g23100 | A01 | 11806943 | C | T | missense_variant | MODERATE | c.956C>T|p.Ala319Val |
S242 |
| 34224 | BAA01g23100 | A01 | 11807096 | G | A | missense_variant | MODERATE | c.1109G>A|p.Gly370Glu |
S301 S304 |
| 34225 | BAA01g23100 | A01 | 11807602 | C | T | missense_variant | MODERATE | c.1615C>T|p.Leu539Phe |
S139 |