| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 120651 | BAA10g11930 | A10 | 13493097 | G | A | upstream_gene_variant | MODIFIER | c.-1198C>T| |
S205 |
| 120652 | BAA10g11930 | A10 | 13493136 | G | A | upstream_gene_variant | MODIFIER | c.-1237C>T| |
S221 |
| 120653 | BAA10g11930 | A10 | 13493308 | C | T | upstream_gene_variant | MODIFIER | c.-1409G>A| |
S305 |
| 120654 | BAA10g11930 | A10 | 13495732 | G | A | upstream_gene_variant | MODIFIER | c.-3833C>T| |
S288 |
| 120655 | BAA10g11930 | A10 | 13496359 | T | A | upstream_gene_variant | MODIFIER | c.-4460A>T| |
S247 |
| 120656 | BAA10g11930-BAA10g11940 | A10 | 13497877 | C | T | intergenic_region | MODIFIER | n.13497877C>T| |
S210 S225 |
| 120657 | BAA10g11940 | A10 | 13501643 | C | T | downstream_gene_variant | MODIFIER | c.*2257G>A| |
S46 |
| 120658 | BAA10g11940 | A10 | 13501648 | G | A | downstream_gene_variant | MODIFIER | c.*2252C>T| |
S192 |
| 120659 | BAA10g11940 | A10 | 13502662 | G | A | downstream_gene_variant | MODIFIER | c.*1238C>T| |
S33 |
| 120660 | BAA10g11940 | A10 | 13502726 | G | A | downstream_gene_variant | MODIFIER | c.*1174C>T| |
S43 |
| 120661 | BAA10g11940 | A10 | 13502730 | C | T | downstream_gene_variant | MODIFIER | c.*1170G>A| |
S200 |
| 120662 | BAA10g11940 | A10 | 13503860 | C | T | downstream_gene_variant | MODIFIER | c.*40G>A| |
S119 |
| 120663 | BAA10g11940 | A10 | 13504319 | G | A | missense_variant | MODERATE | c.145C>T|p.Leu49Phe |
S79 S84 |
| 120664 | BAA10g11940 | A10 | 13504414 | C | T | missense_variant | MODERATE | c.50G>A|p.Gly17Glu |
S297 |
| 120665 | BAA10g11940 | A10 | 13504458 | C | T | synonymous_variant | LOW | c.6G>A|p.Glu2Glu |
S86 |
| 120666 | BAA10g11940 | A10 | 13505996 | C | A | upstream_gene_variant | MODIFIER | c.-1533G>T| |
S235 S236 S260 |
| 120667 | BAA10g11940 | A10 | 13506029 | G | A | upstream_gene_variant | MODIFIER | c.-1566C>T| |
S13 |
| 120668 | BAA10g11940 | A10 | 13506611 | C | T | upstream_gene_variant | MODIFIER | c.-2148G>A| |
S191 |
| 120669 | BAA10g11940 | A10 | 13506669 | G | A | upstream_gene_variant | MODIFIER | c.-2206C>T| |
S57 |
| 120670 | BAA10g11940 | A10 | 13507492 | G | A | upstream_gene_variant | MODIFIER | c.-3029C>T| |
S9 |
| 120671 | BAA10g11940 | A10 | 13507613 | G | A | upstream_gene_variant | MODIFIER | c.-3150C>T| |
S308 |
| 120672 | BAA10g11950 | A10 | 13508296 | G | A | missense_variant | MODERATE | c.740C>T|p.Thr247Ile |
S65 |
| 120673 | BAA10g11950 | A10 | 13508896 | G | A | missense_variant | MODERATE | c.140C>T|p.Pro47Leu |
S65 |
| 120674 | BAA10g11950 | A10 | 13509519 | C | T | upstream_gene_variant | MODIFIER | c.-484G>A| |
S249 |
| 120675 | BAA10g11950 | A10 | 13509659 | C | T | upstream_gene_variant | MODIFIER | c.-624G>A| |
S200 |