| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 86951 | BAA01g46250 | A01 | 30868894 | G | A | missense_variant | MODERATE | c.455C>T|p.Ser152Leu |
S124 |
| 86952 | BAA01g46230 | A01 | 30868998 | G | A | downstream_gene_variant | MODIFIER | c.*4395G>A| |
S173 |
| 86953 | BAA01g46250 | A01 | 30870336 | G | A | upstream_gene_variant | MODIFIER | c.-521C>T| |
S136 |
| 86954 | BAA01g46250 | A01 | 30870459 | G | A | upstream_gene_variant | MODIFIER | c.-644C>T| |
S262 |
| 86955 | BAA01g46260 | A01 | 30870814 | G | A | missense_variant | MODERATE | c.3377C>T|p.Ala1126Val |
S291 |
| 86956 | BAA01g46260 | A01 | 30871029 | C | T | missense_variant | MODERATE | c.3162G>A|p.Met1054Ile |
S8 |
| 86957 | BAA01g46260 | A01 | 30871212 | C | T | stop_gained | HIGH | c.2979G>A|p.Trp993* |
S8 |
| 86958 | BAA01g46260 | A01 | 30871484 | C | T | missense_variant | MODERATE | c.2707G>A|p.Glu903Lys |
S78 S83 |
| 86959 | BAA01g46260 | A01 | 30871511 | C | T | missense_variant | MODERATE | c.2680G>A|p.Val894Ile |
S77 S82 |
| 86960 | BAA01g46260 | A01 | 30871543 | G | A | missense_variant | MODERATE | c.2648C>T|p.Ala883Val |
S284 |
| 86961 | BAA01g46260 | A01 | 30871826 | C | T | missense_variant | MODERATE | c.2365G>A|p.Val789Ile |
S75 S81 |
| 86962 | BAA01g46260 | A01 | 30871962 | C | T | synonymous_variant | LOW | c.2229G>A|p.Lys743Lys |
S57 |
| 86963 | BAA01g46250 | A01 | 30872941 | C | T | upstream_gene_variant | MODIFIER | c.-3126G>A| |
S18 |
| 86964 | BAA01g46260 | A01 | 30873625 | G | A | missense_variant | MODERATE | c.1036C>T|p.Leu346Phe |
S140 |
| 86965 | BAA01g46250 | A01 | 30873914 | C | T | upstream_gene_variant | MODIFIER | c.-4099G>A| |
S41 |
| 86966 | BAA01g46260 | A01 | 30874583 | C | T | synonymous_variant | LOW | c.312G>A|p.Thr104Thr |
S112 |
| 86967 | BAA01g46260 | A01 | 30874682 | C | T | synonymous_variant | LOW | c.213G>A|p.Pro71Pro |
S221 |
| 86968 | BAA01g46260 | A01 | 30874781 | C | T | synonymous_variant | LOW | c.114G>A|p.Arg38Arg |
S60 |
| 86969 | BAA01g46270 | A01 | 30877416 | C | T | missense_variant | MODERATE | c.772G>A|p.Val258Met |
S249 |
| 86970 | BAA01g46270 | A01 | 30877748 | G | A | missense_variant | MODERATE | c.440C>T|p.Thr147Ile |
S143 |
| 86971 | BAA01g46260 | A01 | 30878276 | C | T | upstream_gene_variant | MODIFIER | c.-3382G>A| |
S32 |
| 86972 | BAA01g46290 | A01 | 30881059 | C | T | missense_variant | MODERATE | c.400G>A|p.Glu134Lys |
S235 |
| 86973 | BAA01g46290 | A01 | 30881074 | C | T | missense_variant | MODERATE | c.385G>A|p.Ala129Thr |
S16 |
| 86974 | BAA01g46290 | A01 | 30881094 | G | A | missense_variant | MODERATE | c.365C>T|p.Ser122Leu |
S257 |
| 86975 | BAA01g46290 | A01 | 30881131 | C | T | missense_variant | MODERATE | c.328G>A|p.Gly110Arg |
S1 S90 |