| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 100051 | BAA10g06770 | A10 | 3631775 | C | T | synonymous_variant | LOW | c.1284G>A|p.Leu428Leu |
S246 |
| 100052 | BAA10g06760 | A10 | 3632587 | G | A | downstream_gene_variant | MODIFIER | c.*2113G>A| |
S80 |
| 100053 | BAA10g06760 | A10 | 3632997 | G | A | downstream_gene_variant | MODIFIER | c.*2523G>A| |
S211 S227 |
| 100054 | BAA10g06770 | A10 | 3634299 | C | T | missense_variant | MODERATE | c.25G>A|p.Glu9Lys |
S176 |
| 100055 | BAA10g06770 | A10 | 3635367 | G | A | upstream_gene_variant | MODIFIER | c.-1044C>T| |
S296 |
| 100056 | BAA10g06770 | A10 | 3637285 | G | A | upstream_gene_variant | MODIFIER | c.-2962C>T| |
S295 |
| 100057 | BAA10g06770 | A10 | 3637935 | G | A | upstream_gene_variant | MODIFIER | c.-3612C>T| |
S13 |
| 100058 | BAA10g06790 | A10 | 3639050 | G | A | stop_gained | HIGH | c.796C>T|p.Gln266* |
S157 S163 |
| 100059 | BAA10g06790 | A10 | 3639223 | G | A | missense_variant | MODERATE | c.623C>T|p.Ser208Phe |
S55 |
| 100060 | BAA10g06790 | A10 | 3639396 | G | A | missense_variant | MODERATE | c.542C>T|p.Thr181Ile |
S217 |
| 100061 | BAA10g06780 | A10 | 3640130 | C | T | upstream_gene_variant | MODIFIER | c.-1760G>A| |
S169 |
| 100062 | BAA10g06780 | A10 | 3640256 | G | A | upstream_gene_variant | MODIFIER | c.-1886C>T| |
S161 |
| 100063 | BAA10g06780 | A10 | 3640400 | C | T | upstream_gene_variant | MODIFIER | c.-2030G>A| |
S208 S93 |
| 100064 | BAA10g06780 | A10 | 3640642 | G | A | upstream_gene_variant | MODIFIER | c.-2272C>T| |
S58 |
| 100065 | BAA10g06780 | A10 | 3641634 | C | T | upstream_gene_variant | MODIFIER | c.-3264G>A| |
S34 |
| 100066 | BAA10g06780 | A10 | 3642747 | G | A | upstream_gene_variant | MODIFIER | c.-4377C>T| |
S234 |
| 100067 | BAA10g06790 | A10 | 3644023 | C | T | upstream_gene_variant | MODIFIER | c.-3923G>A| |
S169 |
| 100068 | BAA10g06790 | A10 | 3644202 | G | A | upstream_gene_variant | MODIFIER | c.-4102C>T| |
S202 |
| 100069 | BAA10g06790 | A10 | 3644235 | G | A | upstream_gene_variant | MODIFIER | c.-4135C>T| |
S59 |
| 100070 | BAA10g06810 | A10 | 3645167 | C | T | upstream_gene_variant | MODIFIER | c.-847C>T| |
S224 |
| 100071 | BAA10g06810 | A10 | 3645790 | C | T | upstream_gene_variant | MODIFIER | c.-224C>T| |
S185 |
| 100072 | BAA10g06810 | A10 | 3646045 | G | A | missense_variant&splice_region_variant | MODERATE | c.32G>A|p.Arg11Lys |
S105 S106 |
| 100073 | BAA10g06800 | A10 | 3646056 | C | T | downstream_gene_variant | MODIFIER | c.*3311C>T| |
S47 |
| 100074 | BAA10g06800 | A10 | 3646324 | G | A | downstream_gene_variant | MODIFIER | c.*3579G>A| |
S53 |
| 100075 | BAA10g06800 | A10 | 3647626 | C | T | downstream_gene_variant | MODIFIER | c.*4881C>T| |
S78 S83 |