Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11490 | A10 | 13079754 | G | A | upstream_gene_variant | MODIFIER | c.-4504G>A| |
S245 |
2 | BAA10g11490 | A10 | 13079805 | C | T | upstream_gene_variant | MODIFIER | c.-4453C>T| |
S270 |
3 | BAA10g11490 | A10 | 13079843 | C | T | upstream_gene_variant | MODIFIER | c.-4415C>T| |
S47 |
4 | BAA10g11490 | A10 | 13079855 | G | A | upstream_gene_variant | MODIFIER | c.-4403G>A| |
S9 |
5 | BAA10g11490 | A10 | 13080882 | G | A | upstream_gene_variant | MODIFIER | c.-3376G>A| |
S245 |
6 | BAA10g11490 | A10 | 13081039 | C | T | upstream_gene_variant | MODIFIER | c.-3219C>T| |
S79 S91 |
7 | BAA10g11490 | A10 | 13082105 | G | A | upstream_gene_variant | MODIFIER | c.-2153G>A| |
S148 S30 S31 |
8 | BAA10g11490 | A10 | 13082479 | G | A | upstream_gene_variant | MODIFIER | c.-1779G>A| |
S252 |
9 | BAA10g11490 | A10 | 13082553 | C | T | upstream_gene_variant | MODIFIER | c.-1705C>T| |
S200 |
10 | BAA10g11490 | A10 | 13082565 | C | T | upstream_gene_variant | MODIFIER | c.-1693C>T| |
S167 |
11 | BAA10g11490 | A10 | 13083920 | C | T | upstream_gene_variant | MODIFIER | c.-338C>T| |
S73 S91 |
12 | BAA10g11490 | A10 | 13085537 | C | T | missense_variant | MODERATE | c.686C>T|p.Pro229Leu |
S121 |
13 | BAA10g11490 | A10 | 13085650 | C | T | intron_variant | MODIFIER | c.718-14C>T| |
S301 S304 |
14 | BAA10g11490 | A10 | 13085925 | C | T | downstream_gene_variant | MODIFIER | c.*35C>T| |
S162 |
15 | BAA10g11490 | A10 | 13086123 | G | A | downstream_gene_variant | MODIFIER | c.*233G>A| |
S1 S90 |
16 | BAA10g11490 | A10 | 13086643 | C | T | downstream_gene_variant | MODIFIER | c.*753C>T| |
S190 |
17 | BAA10g11490 | A10 | 13086977 | C | T | downstream_gene_variant | MODIFIER | c.*1087C>T| |
S84 S93 |
18 | BAA10g11490 | A10 | 13087129 | C | T | downstream_gene_variant | MODIFIER | c.*1239C>T| |
S2 |
19 | BAA10g11490 | A10 | 13088103 | G | A | downstream_gene_variant | MODIFIER | c.*2213G>A| |
S140 |
20 | BAA10g11490 | A10 | 13088810 | G | A | downstream_gene_variant | MODIFIER | c.*2920G>A| |
S125 |