| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 144651 | BAA10g29310 | A10 | 22112097 | C | T | upstream_gene_variant | MODIFIER | c.-2518G>A| |
S153 S213 |
| 144652 | BAA10g29310 | A10 | 22112820 | C | T | upstream_gene_variant | MODIFIER | c.-3241G>A| |
S308 |
| 144653 | BAA10g29330 | A10 | 22113841 | C | T | missense_variant | MODERATE | c.1732G>A|p.Gly578Ser |
S218 |
| 144654 | BAA10g29330 | A10 | 22114146 | C | T | stop_gained | HIGH | c.1551G>A|p.Trp517* |
S44 |
| 144655 | BAA10g29330 | A10 | 22114904 | G | A | synonymous_variant | LOW | c.1065C>T|p.Phe355Phe |
S179 |
| 144656 | BAA10g29330 | A10 | 22115154 | C | T | synonymous_variant | LOW | c.897G>A|p.Gln299Gln |
S306 S308 |
| 144657 | BAA10g29330 | A10 | 22115183 | C | T | missense_variant | MODERATE | c.868G>A|p.Val290Ile |
S204 |
| 144658 | BAA10g29320 | A10 | 22115559 | C | T | upstream_gene_variant | MODIFIER | c.-4409G>A| |
S20 |
| 144659 | BAA10g29330 | A10 | 22116019 | C | A | stop_gained | HIGH | c.460G>T|p.Glu154* |
S11 |
| 144660 | BAA10g29330 | A10 | 22116553 | C | T | missense_variant | MODERATE | c.79G>A|p.Gly27Ser |
S161 |
| 144661 | BAA10g29330 | A10 | 22116777 | T | G | upstream_gene_variant | MODIFIER | c.-146A>C| |
S143 |
| 144662 | BAA10g29340 | A10 | 22117195 | G | A | missense_variant | MODERATE | c.71G>A|p.Arg24Lys |
S134 |
| 144663 | BAA10g29350 | A10 | 22118130 | G | A | synonymous_variant | LOW | c.3477C>T|p.Ile1159Ile |
S203 |
| 144664 | BAA10g29330 | A10 | 22118342 | G | A | upstream_gene_variant | MODIFIER | c.-1711C>T| |
S180 |
| 144665 | BAA10g29330 | A10 | 22118771 | G | A | upstream_gene_variant | MODIFIER | c.-2140C>T| |
S94 |
| 144666 | BAA10g29330 | A10 | 22119943 | G | A | upstream_gene_variant | MODIFIER | c.-3312C>T| |
S4 |
| 144667 | BAA10g29350 | A10 | 22120885 | G | A | synonymous_variant | LOW | c.2887C>T|p.Leu963Leu |
S200 |
| 144668 | BAA10g29350 | A10 | 22121007 | G | A | missense_variant | MODERATE | c.2846C>T|p.Thr949Ile |
S219 S72 |
| 144669 | BAA10g29350 | A10 | 22123495 | G | A | missense_variant | MODERATE | c.1745C>T|p.Pro582Leu |
S136 |
| 144670 | BAA10g29350 | A10 | 22123532 | G | A | missense_variant | MODERATE | c.1708C>T|p.Pro570Ser |
S88 |
| 144671 | BAA10g29360 | A10 | 22123630 | G | A | downstream_gene_variant | MODIFIER | c.*3094C>T| |
S61 |
| 144672 | BAA10g29360 | A10 | 22123696 | C | T | downstream_gene_variant | MODIFIER | c.*3028G>A| |
S221 |
| 144673 | BAA10g29350 | A10 | 22125103 | G | A | synonymous_variant | LOW | c.783C>T|p.Asn261Asn |
S231 |
| 144674 | BAA10g29360 | A10 | 22128058 | G | A | missense_variant | MODERATE | c.301C>T|p.Pro101Ser |
S178 |
| 144675 | BAA10g29360 | A10 | 22128691 | C | T | missense_variant | MODERATE | c.58G>A|p.Val20Ile |
S238 |