| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 156001 | BAA02g04090 | A02 | 1776286 | G | A | missense_variant&splice_region_variant | MODERATE | c.343G>A|p.Ala115Thr |
S25 |
| 156002 | BAA02g04070 | A02 | 1777178 | C | T | downstream_gene_variant | MODIFIER | c.*3585C>T| |
S108 |
| 156003 | BAA02g04070 | A02 | 1777212 | C | T | downstream_gene_variant | MODIFIER | c.*3619C>T| |
S245 |
| 156004 | BAA02g04070 | A02 | 1777768 | G | A | downstream_gene_variant | MODIFIER | c.*4175G>A| |
S139 |
| 156005 | BAA02g04070 | A02 | 1778187 | C | T | downstream_gene_variant | MODIFIER | c.*4594C>T| |
S144 |
| 156006 | BAA02g04100 | A02 | 1779449 | G | A | upstream_gene_variant | MODIFIER | c.-101C>T| |
S140 |
| 156007 | BAA02g04100 | A02 | 1781562 | C | T | upstream_gene_variant | MODIFIER | c.-2214G>A| |
S245 |
| 156008 | BAA02g04100 | A02 | 1782827 | A | C | upstream_gene_variant | MODIFIER | c.-3479T>G| |
S108 |
| 156009 | BAA02g04110 | A02 | 1783936 | C | T | synonymous_variant | LOW | c.1239G>A|p.Lys413Lys |
S40 S49 |
| 156010 | BAA02g04110 | A02 | 1785451 | C | T | splice_region_variant&intron_variant | LOW | c.619+8G>A| |
S108 |
| 156011 | BAA02g04110 | A02 | 1785468 | C | T | missense_variant | MODERATE | c.610G>A|p.Glu204Lys |
S100 |
| 156012 | BAA02g04120 | A02 | 1785739 | G | A | upstream_gene_variant | MODIFIER | c.-1495G>A| |
S274 S279 |
| 156013 | BAA02g04120 | A02 | 1785754 | A | G | upstream_gene_variant | MODIFIER | c.-1480A>G| |
S274 |
| 156014 | BAA02g04120 | A02 | 1785757 | A | G | upstream_gene_variant | MODIFIER | c.-1477A>G| |
S274 |
| 156015 | BAA02g04110 | A02 | 1785858 | G | A | synonymous_variant | LOW | c.313C>T|p.Leu105Leu |
S208 |
| 156016 | BAA02g04110 | A02 | 1786529 | G | A | synonymous_variant | LOW | c.72C>T|p.Val24Val |
S295 |
| 156017 | BAA02g04110 | A02 | 1786570 | C | T | missense_variant | MODERATE | c.31G>A|p.Glu11Lys |
S159 |
| 156018 | BAA02g04120 | A02 | 1787329 | C | T | synonymous_variant | LOW | c.96C>T|p.Asn32Asn |
S251 |
| 156019 | BAA02g04120 | A02 | 1787598 | C | T | missense_variant | MODERATE | c.209C>T|p.Ser70Phe |
S211 |
| 156020 | BAA02g04110 | A02 | 1787929 | G | A | upstream_gene_variant | MODIFIER | c.-1329C>T| |
S44 |
| 156021 | BAA02g04110 | A02 | 1788805 | G | A | upstream_gene_variant | MODIFIER | c.-2205C>T| |
S162 |
| 156022 | BAA02g04120 | A02 | 1790014 | G | A | synonymous_variant | LOW | c.1176G>A|p.Val392Val |
S140 |
| 156023 | BAA02g04110 | A02 | 1790545 | G | A | upstream_gene_variant | MODIFIER | c.-3945C>T| |
S295 |
| 156024 | BAA02g04130 | A02 | 1792645 | G | A | synonymous_variant | LOW | c.954C>T|p.Phe318Phe |
S287 |
| 156025 | BAA02g04140 | A02 | 1796251 | C | T | missense_variant | MODERATE | c.436G>A|p.Val146Ile |
S38 |