| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 143601 | BAA10g28400 | A10 | 21764459 | C | T | upstream_gene_variant | MODIFIER | c.-2518G>A| |
S8 |
| 143602 | BAA10g28400 | A10 | 21765477 | G | A | upstream_gene_variant | MODIFIER | c.-3536C>T| |
S263 |
| 143603 | BAA10g28410 | A10 | 21766635 | C | T | missense_variant&splice_region_variant | MODERATE | c.1534G>A|p.Ala512Thr |
S224 |
| 143604 | BAA10g28410 | A10 | 21766876 | C | T | synonymous_variant | LOW | c.1293G>A|p.Glu431Glu |
S136 |
| 143605 | BAA10g28410 | A10 | 21767350 | G | A | missense_variant | MODERATE | c.1216C>T|p.Leu406Phe |
S131 |
| 143606 | BAA10g28410 | A10 | 21768330 | G | A | missense_variant | MODERATE | c.569C>T|p.Thr190Ile |
S262 |
| 143607 | BAA10g28410 | A10 | 21768866 | C | T | synonymous_variant | LOW | c.243G>A|p.Lys81Lys |
S5 |
| 143608 | BAA10g28410 | A10 | 21769527 | C | T | upstream_gene_variant | MODIFIER | c.-419G>A| |
S36 |
| 143609 | BAA10g28420 | A10 | 21769613 | C | T | missense_variant | MODERATE | c.1136G>A|p.Gly379Glu |
S268 |
| 143610 | BAA10g28420 | A10 | 21770610 | G | A | missense_variant | MODERATE | c.139C>T|p.Pro47Ser |
S208 |
| 143611 | BAA10g28410 | A10 | 21771399 | C | T | upstream_gene_variant | MODIFIER | c.-2291G>A| |
S121 |
| 143612 | BAA10g28410 | A10 | 21771420 | G | A | upstream_gene_variant | MODIFIER | c.-2312C>T| |
S106 |
| 143613 | BAA10g28410 | A10 | 21772154 | C | T | upstream_gene_variant | MODIFIER | c.-3046G>A| |
S133 |
| 143614 | BAA10g28420 | A10 | 21775172 | C | T | upstream_gene_variant | MODIFIER | c.-4424G>A| |
S153 S213 |
| 143615 | BAA10g28420 | A10 | 21775257 | C | T | upstream_gene_variant | MODIFIER | c.-4509G>A| |
S295 |
| 143616 | BAA10g28420 | A10 | 21775561 | C | T | upstream_gene_variant | MODIFIER | c.-4813G>A| |
S210 |
| 143617 | BAA10g28430 | A10 | 21775788 | C | T | upstream_gene_variant | MODIFIER | c.-829C>T| |
S68 |
| 143618 | BAA10g28430 | A10 | 21776002 | C | T | upstream_gene_variant | MODIFIER | c.-615C>T| |
S2 |
| 143619 | BAA10g28430 | A10 | 21776702 | C | T | missense_variant | MODERATE | c.86C>T|p.Ala29Val |
S259 |
| 143620 | BAA10g28440 | A10 | 21778686 | G | A | upstream_gene_variant | MODIFIER | c.-2978G>A| |
S278 |
| 143621 | BAA10g28440 | A10 | 21779406 | G | A | upstream_gene_variant | MODIFIER | c.-2258G>A| |
S127 |
| 143622 | BAA10g28440 | A10 | 21779688 | C | T | upstream_gene_variant | MODIFIER | c.-1976C>T| |
S301 S304 |
| 143623 | BAA10g28440 | A10 | 21780631 | G | A | upstream_gene_variant | MODIFIER | c.-1033G>A| |
S181 |
| 143624 | BAA10g28440 | A10 | 21780730 | C | T | upstream_gene_variant | MODIFIER | c.-934C>T| |
S13 S168 S219 S279 S72 |
| 143625 | BAA10g28440 | A10 | 21781346 | G | A | upstream_gene_variant | MODIFIER | c.-318G>A| |
S199 |