| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 70551 | BAA01g36950 | A01 | 24691245 | G | A | upstream_gene_variant | MODIFIER | c.-4819G>A| |
S284 |
| 70552 | BAA01g36950 | A01 | 24691684 | G | A | upstream_gene_variant | MODIFIER | c.-4380G>A| |
S246 |
| 70553 | BAA01g36950 | A01 | 24692196 | G | A | upstream_gene_variant | MODIFIER | c.-3868G>A| |
S287 |
| 70554 | BAA01g36950 | A01 | 24694022 | C | T | upstream_gene_variant | MODIFIER | c.-2042C>T| |
S228 |
| 70555 | BAA01g36950 | A01 | 24695387 | C | T | upstream_gene_variant | MODIFIER | c.-677C>T| |
S295 |
| 70556 | BAA01g36950 | A01 | 24695716 | G | A | upstream_gene_variant | MODIFIER | c.-348G>A| |
S68 |
| 70557 | BAA01g36950 | A01 | 24696129 | C | T | synonymous_variant | LOW | c.66C>T|p.Ala22Ala |
S242 |
| 70558 | BAA01g36950 | A01 | 24697729 | C | T | downstream_gene_variant | MODIFIER | c.*682C>T| |
S262 |
| 70559 | BAA01g36960 | A01 | 24698863 | C | T | missense_variant | MODERATE | c.253G>A|p.Glu85Lys |
S170 |
| 70560 | BAA01g36960 | A01 | 24699425 | C | T | upstream_gene_variant | MODIFIER | c.-224G>A| |
S153 |
| 70561 | BAA01g36960 | A01 | 24702840 | G | A | upstream_gene_variant | MODIFIER | c.-3639C>T| |
S172 S217 |
| 70562 | BAA01g36960 | A01 | 24703003 | G | A | upstream_gene_variant | MODIFIER | c.-3802C>T| |
S163 |
| 70563 | BAA01g36960 | A01 | 24703493 | C | T | upstream_gene_variant | MODIFIER | c.-4292G>A| |
S301 S304 |
| 70564 | BAA01g36980 | A01 | 24708328 | C | T | upstream_gene_variant | MODIFIER | c.-209C>T| |
S235 |
| 70565 | BAA01g36980 | A01 | 24708603 | C | T | synonymous_variant | LOW | c.67C>T|p.Leu23Leu |
S242 |
| 70566 | BAA01g36980 | A01 | 24709415 | C | T | missense_variant | MODERATE | c.314C>T|p.Thr105Ile |
S230 |
| 70567 | BAA01g36970 | A01 | 24709993 | C | T | downstream_gene_variant | MODIFIER | c.*4378C>T| |
S80 |
| 70568 | BAA01g36980 | A01 | 24710982 | G | A | downstream_gene_variant | MODIFIER | c.*1389G>A| |
S223 |
| 70569 | BAA01g36980 | A01 | 24712867 | C | T | downstream_gene_variant | MODIFIER | c.*3274C>T| |
S57 |
| 70570 | BAA01g36990 | A01 | 24714658 | G | A | upstream_gene_variant | MODIFIER | c.-4075G>A| |
S262 |
| 70571 | BAA01g36990 | A01 | 24718936 | C | T | synonymous_variant | LOW | c.204C>T|p.Asp68Asp |
S98 |
| 70572 | BAA01g36990 | A01 | 24718956 | G | A | missense_variant | MODERATE | c.224G>A|p.Gly75Asp |
S229 |
| 70573 | BAA01g36990 | A01 | 24719593 | G | A | synonymous_variant | LOW | c.861G>A|p.Ala287Ala |
S223 |
| 70574 | BAA01g36990 | A01 | 24719724 | G | A | intron_variant | MODIFIER | c.938+54G>A| |
S175 |
| 70575 | BAA01g36990 | A01 | 24720570 | C | T | intron_variant | MODIFIER | c.938+900C>T| |
S192 |