| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 87351 | BAA01g46520 | A01 | 31004762 | C | T | upstream_gene_variant | MODIFIER | c.-732G>A| |
S13 |
| 87352 | BAA01g46520 | A01 | 31004805 | C | T | upstream_gene_variant | MODIFIER | c.-775G>A| |
S70 |
| 87353 | BAA01g46530 | A01 | 31005288 | C | T | synonymous_variant | LOW | c.1482G>A|p.Lys494Lys |
S223 |
| 87354 | BAA01g46530 | A01 | 31005616 | C | T | missense_variant | MODERATE | c.1154G>A|p.Arg385Lys |
S252 |
| 87355 | BAA01g46530 | A01 | 31006563 | C | T | synonymous_variant | LOW | c.207G>A|p.Glu69Glu |
S99 |
| 87356 | BAA01g46520 | A01 | 31006924 | G | A | upstream_gene_variant | MODIFIER | c.-2894C>T| |
S42 |
| 87357 | BAA01g46540 | A01 | 31007843 | G | A | missense_variant | MODERATE | c.295G>A|p.Gly99Arg |
S164 |
| 87358 | BAA01g46540 | A01 | 31007844 | G | A | missense_variant | MODERATE | c.296G>A|p.Gly99Glu |
S35 |
| 87359 | BAA01g46540 | A01 | 31008492 | G | A | missense_variant | MODERATE | c.749G>A|p.Gly250Glu |
S273 |
| 87360 | BAA01g46550 | A01 | 31009647 | C | T | missense_variant | MODERATE | c.692G>A|p.Arg231Lys |
S202 |
| 87361 | BAA01g46550 | A01 | 31010168 | C | T | synonymous_variant | LOW | c.171G>A|p.Leu57Leu |
S302 |
| 87362 | BAA01g46530 | A01 | 31010342 | G | A | upstream_gene_variant | MODIFIER | c.-3573C>T| |
S260 |
| 87363 | BAA01g46530 | A01 | 31010626 | C | T | upstream_gene_variant | MODIFIER | c.-3857G>A| |
S103 |
| 87364 | BAA01g46530 | A01 | 31010734 | G | A | upstream_gene_variant | MODIFIER | c.-3965C>T| |
S9 |
| 87365 | BAA01g46560 | A01 | 31011142 | G | A | missense_variant | MODERATE | c.4G>A|p.Glu2Lys |
S177 S64 |
| 87366 | BAA01g46550 | A01 | 31012783 | C | T | upstream_gene_variant | MODIFIER | c.-1937G>A| |
|
| 87367 | BAA01g46560 | A01 | 31012994 | G | A | synonymous_variant | LOW | c.1365G>A|p.Arg455Arg |
S191 |
| 87368 | BAA01g46550 | A01 | 31014140 | C | T | upstream_gene_variant | MODIFIER | c.-3294G>A| |
S212 |
| 87369 | BAA01g46550 | A01 | 31014323 | G | A | upstream_gene_variant | MODIFIER | c.-3477C>T| |
S288 |
| 87370 | BAA01g46550 | A01 | 31015121 | G | A | upstream_gene_variant | MODIFIER | c.-4275C>T| |
S282 |
| 87371 | BAA01g46570 | A01 | 31015221 | C | T | missense_variant | MODERATE | c.319G>A|p.Val107Met |
S5 |
| 87372 | BAA01g46570 | A01 | 31016315 | G | A | upstream_gene_variant | MODIFIER | c.-607C>T| |
S146 |
| 87373 | BAA01g46570 | A01 | 31016575 | G | A | upstream_gene_variant | MODIFIER | c.-867C>T| |
S73 |
| 87374 | BAA01g46570 | A01 | 31016647 | G | A | upstream_gene_variant | MODIFIER | c.-939C>T| |
S47 |
| 87375 | BAA01g46570 | A01 | 31017046 | G | A | upstream_gene_variant | MODIFIER | c.-1338C>T| |
S68 |