| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 54901 | BAA01g30000 | A01 | 19032539 | C | T | upstream_gene_variant | MODIFIER | c.-4468C>T| |
S81 S85 |
| 54902 | BAA01g29980 | A01 | 19033669 | G | A | upstream_gene_variant | MODIFIER | c.-89C>T| |
S268 |
| 54903 | BAA01g29980 | A01 | 19033975 | G | A | upstream_gene_variant | MODIFIER | c.-395C>T| |
S43 |
| 54904 | BAA01g29980 | A01 | 19034339 | C | T | upstream_gene_variant | MODIFIER | c.-759G>A| |
S10 |
| 54905 | BAA01g29980 | A01 | 19034690 | G | A | upstream_gene_variant | MODIFIER | c.-1110C>T| |
S247 |
| 54906 | BAA01g29980 | A01 | 19034807 | C | T | upstream_gene_variant | MODIFIER | c.-1227G>A| |
S107 |
| 54907 | BAA01g29990 | A01 | 19035934 | C | T | missense_variant | MODERATE | c.292G>A|p.Ala98Thr |
S270 |
| 54908 | BAA01g29990 | A01 | 19036153 | C | T | missense_variant | MODERATE | c.73G>A|p.Ala25Thr |
S189 |
| 54909 | BAA01g29980 | A01 | 19036594 | G | A | upstream_gene_variant | MODIFIER | c.-3014C>T| |
S61 |
| 54910 | BAA01g29980 | A01 | 19036930 | C | T | upstream_gene_variant | MODIFIER | c.-3350G>A| |
S132 S137 S215 S237 S288 S56 S89 |
| 54911 | BAA01g29980 | A01 | 19038464 | G | A | upstream_gene_variant | MODIFIER | c.-4884C>T| |
S25 |
| 54912 | BAA01g29990 | A01 | 19038797 | C | T | upstream_gene_variant | MODIFIER | c.-2572G>A| |
S277 |
| 54913 | BAA01g29990 | A01 | 19039193 | G | A | upstream_gene_variant | MODIFIER | c.-2968C>T| |
S199 |
| 54914 | BAA01g29990 | A01 | 19040718 | C | T | upstream_gene_variant | MODIFIER | c.-4493G>A| |
S160 |
| 54915 | BAA01g30010 | A01 | 19041807 | C | T | splice_donor_variant&intron_variant | HIGH | c.2256+1G>A| |
S65 |
| 54916 | BAA01g30010 | A01 | 19041986 | G | A | missense_variant | MODERATE | c.2078C>T|p.Thr693Ile |
S163 |
| 54917 | BAA01g30010 | A01 | 19042498 | C | T | missense_variant | MODERATE | c.1640G>A|p.Arg547Gln |
S25 S264 |
| 54918 | BAA01g30010 | A01 | 19042675 | C | T | missense_variant | MODERATE | c.1463G>A|p.Gly488Asp |
S277 |
| 54919 | BAA01g30010 | A01 | 19043348 | G | A | missense_variant | MODERATE | c.790C>T|p.Arg264Trp |
S208 |
| 54920 | BAA01g30010 | A01 | 19043409 | C | T | synonymous_variant | LOW | c.729G>A|p.Glu243Glu |
S107 |
| 54921 | BAA01g30010 | A01 | 19043555 | C | T | missense_variant | MODERATE | c.583G>A|p.Glu195Lys |
S267 S48 |
| 54922 | BAA01g30010 | A01 | 19043621 | G | A | missense_variant | MODERATE | c.517C>T|p.Leu173Phe |
S119 |
| 54923 | BAA01g30010 | A01 | 19043851 | G | A | missense_variant | MODERATE | c.287C>T|p.Ser96Phe |
S99 |
| 54924 | BAA01g30010 | A01 | 19045190 | C | T | upstream_gene_variant | MODIFIER | c.-1053G>A| |
S179 |
| 54925 | BAA01g30010 | A01 | 19045836 | G | A | upstream_gene_variant | MODIFIER | c.-1699C>T| |
S207 |