| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 94601 | BAA10g03590 | A10 | 1729459 | G | A | missense_variant | MODERATE | c.136C>T|p.Leu46Phe |
S150 |
| 94602 | BAA10g03580 | A10 | 1729700 | G | A | upstream_gene_variant | MODIFIER | c.-3064C>T| |
S158 |
| 94603 | BAA10g03600 | A10 | 1730250 | G | A | missense_variant | MODERATE | c.992C>T|p.Thr331Ile |
S158 |
| 94604 | BAA10g03600 | A10 | 1730949 | C | T | missense_variant | MODERATE | c.688G>A|p.Asp230Asn |
S297 |
| 94605 | BAA10g03600 | A10 | 1731529 | C | T | synonymous_variant | LOW | c.555G>A|p.Lys185Lys |
S224 |
| 94606 | BAA10g03600 | A10 | 1731581 | G | A | missense_variant | MODERATE | c.503C>T|p.Ala168Val |
S283 |
| 94607 | BAA10g03590 | A10 | 1732103 | G | A | upstream_gene_variant | MODIFIER | c.-2509C>T| |
S282 |
| 94608 | BAA10g03590 | A10 | 1732106 | G | A | upstream_gene_variant | MODIFIER | c.-2512C>T| |
S284 |
| 94609 | BAA10g03600 | A10 | 1732377 | G | A | missense_variant | MODERATE | c.221C>T|p.Thr74Ile |
S20 |
| 94610 | BAA10g03590 | A10 | 1732639 | C | T | upstream_gene_variant | MODIFIER | c.-3045G>A| |
S206 S26 |
| 94611 | BAA10g03600 | A10 | 1732861 | C | T | missense_variant | MODERATE | c.52G>A|p.Val18Met |
S162 |
| 94612 | BAA10g03590 | A10 | 1733549 | G | A | upstream_gene_variant | MODIFIER | c.-3955C>T| |
S295 |
| 94613 | BAA10g03590 | A10 | 1733947 | G | A | upstream_gene_variant | MODIFIER | c.-4353C>T| |
S274 |
| 94614 | BAA10g03610 | A10 | 1734121 | C | T | missense_variant | MODERATE | c.1091G>A|p.Ser364Asn |
S305 |
| 94615 | BAA10g03610 | A10 | 1734273 | C | T | synonymous_variant | LOW | c.939G>A|p.Glu313Glu |
S173 |
| 94616 | BAA10g03600 | A10 | 1734895 | G | A | upstream_gene_variant | MODIFIER | c.-1983C>T| |
S292 |
| 94617 | BAA10g03600 | A10 | 1735320 | G | A | upstream_gene_variant | MODIFIER | c.-2408C>T| |
S296 |
| 94618 | BAA10g03600 | A10 | 1737702 | G | A | upstream_gene_variant | MODIFIER | c.-4790C>T| |
S20 |
| 94619 | BAA10g03620 | A10 | 1739902 | G | A | stop_gained | HIGH | c.36G>A|p.Trp12* |
S306 S308 |
| 94620 | BAA10g03620 | A10 | 1740078 | G | A | missense_variant | MODERATE | c.212G>A|p.Arg71Lys |
S180 |
| 94621 | BAA10g03620 | A10 | 1740185 | G | A | missense_variant | MODERATE | c.319G>A|p.Glu107Lys |
S72 S78 |
| 94622 | BAA10g03620 | A10 | 1740287 | G | A | missense_variant | MODERATE | c.421G>A|p.Glu141Lys |
S13 |
| 94623 | BAA10g03610 | A10 | 1740694 | G | A | upstream_gene_variant | MODIFIER | c.-4972C>T| |
S205 |
| 94624 | BAA10g03620 | A10 | 1740772 | G | A | downstream_gene_variant | MODIFIER | c.*10G>A| |
S263 |
| 94625 | BAA10g03620 | A10 | 1741156 | G | A | downstream_gene_variant | MODIFIER | c.*394G>A| |
S78 |