| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 153901 | BAA02g02240 | A02 | 1017292 | C | T | downstream_gene_variant | MODIFIER | c.*4885C>T| |
S245 |
| 153902 | BAA02g02260 | A02 | 1018289 | G | A | missense_variant | MODERATE | c.719C>T|p.Ser240Phe |
S165 |
| 153903 | BAA02g02260 | A02 | 1018680 | C | T | missense_variant | MODERATE | c.328G>A|p.Glu110Lys |
S230 |
| 153904 | BAA02g02280 | A02 | 1018755 | C | T | upstream_gene_variant | MODIFIER | c.-4516C>T| |
S32 |
| 153905 | BAA02g02260 | A02 | 1019756 | G | A | upstream_gene_variant | MODIFIER | c.-73C>T| |
S208 S219 |
| 153906 | BAA02g02260 | A02 | 1020167 | G | A | upstream_gene_variant | MODIFIER | c.-484C>T| |
S81 S85 |
| 153907 | BAA02g02260 | A02 | 1020618 | C | T | upstream_gene_variant | MODIFIER | c.-935G>A| |
S250 |
| 153908 | BAA02g02270 | A02 | 1021015 | C | T | missense_variant | MODERATE | c.185G>A|p.Gly62Glu |
S229 |
| 153909 | BAA02g02270 | A02 | 1026179 | G | A | upstream_gene_variant | MODIFIER | c.-4899C>T| |
S107 |
| 153910 | BAA02g02290 | A02 | 1027533 | C | T | upstream_gene_variant | MODIFIER | c.-1748C>T| |
S281 |
| 153911 | BAA02g02290 | A02 | 1029046 | C | T | upstream_gene_variant | MODIFIER | c.-235C>T| |
S187 |
| 153912 | BAA02g02290 | A02 | 1029190 | C | T | upstream_gene_variant | MODIFIER | c.-91C>T| |
S278 |
| 153913 | BAA02g02290 | A02 | 1030034 | G | A | missense_variant | MODERATE | c.604G>A|p.Asp202Asn |
S67 |
| 153914 | BAA02g02290 | A02 | 1030595 | G | A | splice_donor_variant&intron_variant | HIGH | c.772+1G>A| |
S96 |
| 153915 | BAA02g02300 | A02 | 1032775 | C | T | upstream_gene_variant | MODIFIER | c.-170C>T| |
S138 |
| 153916 | BAA02g02300 | A02 | 1034233 | G | A | missense_variant | MODERATE | c.1289G>A|p.Arg430Gln |
S265 |
| 153917 | BAA02g02290 | A02 | 1035330 | G | A | downstream_gene_variant | MODIFIER | c.*3665G>A| |
S157 S166 S167 S236 S262 |
| 153918 | BAA02g02290 | A02 | 1035376 | C | T | downstream_gene_variant | MODIFIER | c.*3711C>T| |
S73 |
| 153919 | BAA02g02290 | A02 | 1035566 | G | A | downstream_gene_variant | MODIFIER | c.*3901G>A| |
S288 |
| 153920 | BAA02g02310 | A02 | 1036985 | G | A | missense_variant | MODERATE | c.2396C>T|p.Ser799Phe |
S163 |
| 153921 | BAA02g02310 | A02 | 1037117 | G | A | missense_variant | MODERATE | c.2264C>T|p.Thr755Met |
S78 |
| 153922 | BAA02g02310 | A02 | 1037346 | C | T | missense_variant | MODERATE | c.2035G>A|p.Glu679Lys |
S58 |
| 153923 | BAA02g02310 | A02 | 1037800 | G | A | synonymous_variant | LOW | c.1581C>T|p.Ile527Ile |
S202 |
| 153924 | BAA02g02310 | A02 | 1038312 | G | A | missense_variant | MODERATE | c.1069C>T|p.Arg357Cys |
S143 |
| 153925 | BAA02g02310 | A02 | 1038313 | C | T | synonymous_variant | LOW | c.1068G>A|p.Ser356Ser |
S61 |