| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 122351 | BAA10g12740 | A10 | 14093638 | C | T | missense_variant | MODERATE | c.358C>T|p.Arg120Cys |
S185 |
| 122352 | BAA10g12740 | A10 | 14093884 | G | A | missense_variant | MODERATE | c.604G>A|p.Gly202Arg |
S65 |
| 122353 | BAA10g12740 | A10 | 14093963 | C | T | missense_variant | MODERATE | c.683C>T|p.Pro228Leu |
S46 |
| 122354 | BAA10g12730 | A10 | 14094065 | C | T | downstream_gene_variant | MODIFIER | c.*1623C>T| |
S195 |
| 122355 | BAA10g12730 | A10 | 14094117 | G | A | downstream_gene_variant | MODIFIER | c.*1675G>A| |
S71 |
| 122356 | BAA10g12730 | A10 | 14094611 | C | T | downstream_gene_variant | MODIFIER | c.*2169C>T| |
S23 |
| 122357 | BAA10g12740 | A10 | 14094875 | G | A | missense_variant | MODERATE | c.842G>A|p.Arg281Lys |
S134 |
| 122358 | BAA10g12730 | A10 | 14095872 | G | A | downstream_gene_variant | MODIFIER | c.*3430G>A| |
S221 |
| 122359 | BAA10g12730 | A10 | 14096256 | C | T | downstream_gene_variant | MODIFIER | c.*3814C>T| |
S187 |
| 122360 | BAA10g12750 | A10 | 14097385 | C | T | missense_variant | MODERATE | c.1541G>A|p.Arg514Gln |
S121 |
| 122361 | BAA10g12750 | A10 | 14097977 | G | A | synonymous_variant | LOW | c.1113C>T|p.Leu371Leu |
S202 |
| 122362 | BAA10g12740 | A10 | 14098138 | C | T | downstream_gene_variant | MODIFIER | c.*2632C>T| |
S188 |
| 122363 | BAA10g12750 | A10 | 14098311 | G | A | missense_variant | MODERATE | c.895C>T|p.Pro299Ser |
S290 |
| 122364 | BAA10g12750 | A10 | 14098314 | C | T | missense_variant | MODERATE | c.892G>A|p.Val298Ile |
S51 |
| 122365 | BAA10g12750 | A10 | 14098344 | G | A | missense_variant | MODERATE | c.862C>T|p.Pro288Ser |
S288 |
| 122366 | BAA10g12750 | A10 | 14098724 | G | A | missense_variant | MODERATE | c.655C>T|p.Leu219Phe |
S251 |
| 122367 | BAA10g12750 | A10 | 14099143 | G | A | missense_variant | MODERATE | c.310C>T|p.His104Tyr |
S78 |
| 122368 | BAA10g12750 | A10 | 14099149 | G | A | synonymous_variant | LOW | c.304C>T|p.Leu102Leu |
S202 |
| 122369 | BAA10g12750 | A10 | 14099822 | G | T | upstream_gene_variant | MODIFIER | c.-370C>A| |
S35 |
| 122370 | BAA10g12750 | A10 | 14100384 | G | A | upstream_gene_variant | MODIFIER | c.-932C>T| |
S158 |
| 122371 | BAA10g12760 | A10 | 14101083 | G | A | missense_variant | MODERATE | c.2156C>T|p.Ala719Val |
S69 |
| 122372 | BAA10g12750 | A10 | 14102721 | C | T | upstream_gene_variant | MODIFIER | c.-3269G>A| |
S155 S211 |
| 122373 | BAA10g12750 | A10 | 14102752 | C | T | upstream_gene_variant | MODIFIER | c.-3300G>A| |
S162 |
| 122374 | BAA10g12750 | A10 | 14102830 | C | T | upstream_gene_variant | MODIFIER | c.-3378G>A| |
S246 |
| 122375 | BAA10g12760 | A10 | 14104057 | C | T | missense_variant | MODERATE | c.1862G>A|p.Gly621Glu |
S87 |