| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 33751 | BAA01g22910 | A01 | 11637793 | G | A | synonymous_variant | LOW | c.5331C>T|p.Leu1777Leu |
S202 |
| 33752 | BAA01g22910 | A01 | 11639301 | C | T | missense_variant | MODERATE | c.4273G>A|p.Glu1425Lys |
S305 |
| 33753 | BAA01g22910 | A01 | 11639681 | G | A | missense_variant | MODERATE | c.3893C>T|p.Ser1298Phe |
S108 |
| 33754 | BAA01g22910 | A01 | 11640149 | C | T | missense_variant | MODERATE | c.3505G>A|p.Glu1169Lys |
S95 |
| 33755 | BAA01g22910 | A01 | 11640303 | G | A | intron_variant | MODIFIER | c.3457+100C>T| |
S94 |
| 33756 | BAA01g22910 | A01 | 11640315 | C | T | intron_variant | MODIFIER | c.3457+88G>A| |
S201 |
| 33757 | BAA01g22910 | A01 | 11640629 | G | A | synonymous_variant | LOW | c.3231C>T|p.Val1077Val |
S172 S217 |
| 33758 | BAA01g22910 | A01 | 11641659 | C | T | intron_variant | MODIFIER | c.2330-129G>A| |
S167 |
| 33759 | BAA01g22910 | A01 | 11642207 | C | T | missense_variant | MODERATE | c.2215G>A|p.Ala739Thr |
S51 |
| 33760 | BAA01g22910 | A01 | 11642299 | G | A | missense_variant | MODERATE | c.2123C>T|p.Ala708Val |
S293 |
| 33761 | BAA01g22910 | A01 | 11642877 | C | T | synonymous_variant | LOW | c.1545G>A|p.Gln515Gln |
S55 |
| 33762 | BAA01g22910 | A01 | 11643016 | G | A | missense_variant | MODERATE | c.1406C>T|p.Pro469Leu |
S212 |
| 33763 | BAA01g22910 | A01 | 11643777 | C | T | synonymous_variant | LOW | c.645G>A|p.Lys215Lys |
S53 |
| 33764 | BAA01g22910 | A01 | 11643924 | C | T | synonymous_variant | LOW | c.498G>A|p.Glu166Glu |
S170 |
| 33765 | BAA01g22910 | A01 | 11644799 | C | T | upstream_gene_variant | MODIFIER | c.-378G>A| |
S69 |
| 33766 | BAA01g22910 | A01 | 11647089 | C | T | upstream_gene_variant | MODIFIER | c.-2668G>A| |
S242 |
| 33767 | BAA01g22910 | A01 | 11647478 | C | T | upstream_gene_variant | MODIFIER | c.-3057G>A| |
S142 |
| 33768 | BAA01g22910 | A01 | 11647608 | C | T | upstream_gene_variant | MODIFIER | c.-3187G>A| |
S140 |
| 33769 | BAA01g22910 | A01 | 11647747 | C | T | upstream_gene_variant | MODIFIER | c.-3326G>A| |
S166 |
| 33770 | BAA01g22910 | A01 | 11647840 | G | A | upstream_gene_variant | MODIFIER | c.-3419C>T| |
S94 |
| 33771 | BAA01g22910 | A01 | 11647984 | C | T | upstream_gene_variant | MODIFIER | c.-3563G>A| |
S211 S227 |
| 33772 | BAA01g22910 | A01 | 11648589 | C | T | upstream_gene_variant | MODIFIER | c.-4168G>A| |
S198 |
| 33773 | BAA01g22920 | A01 | 11650911 | C | T | missense_variant | MODERATE | c.656G>A|p.Gly219Glu |
S90 |
| 33774 | BAA01g22920 | A01 | 11650991 | C | T | synonymous_variant | LOW | c.576G>A|p.Thr192Thr |
S168 |
| 33775 | BAA01g22920 | A01 | 11651052 | G | A | missense_variant | MODERATE | c.515C>T|p.Thr172Met |
S155 S211 |