Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g26400 | A06 | 18066485 | C | T | upstream_gene_variant | MODIFIER | c.-4992C>T| |
S7 |
2 | BAA06g26400 | A06 | 18066697 | G | A | upstream_gene_variant | MODIFIER | c.-4780G>A| |
S69 |
3 | BAA06g26400 | A06 | 18066911 | G | A | upstream_gene_variant | MODIFIER | c.-4566G>A| |
S20 |
4 | BAA06g26400 | A06 | 18067141 | G | A | upstream_gene_variant | MODIFIER | c.-4336G>A| |
S213 |
5 | BAA06g26400 | A06 | 18067354 | G | A | upstream_gene_variant | MODIFIER | c.-4123G>A| |
S95 |
6 | BAA06g26400 | A06 | 18067683 | C | T | upstream_gene_variant | MODIFIER | c.-3794C>T| |
S187 |
7 | BAA06g26400 | A06 | 18067824 | C | T | upstream_gene_variant | MODIFIER | c.-3653C>T| |
S157 |
8 | BAA06g26400 | A06 | 18068218 | G | A | upstream_gene_variant | MODIFIER | c.-3259G>A| |
S209 |
9 | BAA06g26400 | A06 | 18068396 | C | T | upstream_gene_variant | MODIFIER | c.-3081C>T| |
S107 |
10 | BAA06g26400 | A06 | 18068916 | G | A | upstream_gene_variant | MODIFIER | c.-2561G>A| |
S89 |
11 | BAA06g26400 | A06 | 18069172 | G | A | upstream_gene_variant | MODIFIER | c.-2305G>A| |
S177 |
12 | BAA06g26400 | A06 | 18071480 | G | A | missense_variant | MODERATE | c.4G>A|p.Glu2Lys |
S208 S219 |
13 | BAA06g26400 | A06 | 18072993 | T | C | missense_variant | MODERATE | c.887T>C|p.Leu296Pro |
S72 S78 |
14 | BAA06g26400 | A06 | 18073060 | G | A | synonymous_variant | LOW | c.954G>A|p.Gln318Gln |
S63 |
15 | BAA06g26400 | A06 | 18076463 | G | A | downstream_gene_variant | MODIFIER | c.*2678G>A| |
S54 |
16 | BAA06g26400 | A06 | 18076633 | G | A | downstream_gene_variant | MODIFIER | c.*2848G>A| |
S105 S106 |
17 | BAA06g26400 | A06 | 18076640 | G | A | downstream_gene_variant | MODIFIER | c.*2855G>A| |
S67 |
18 | BAA06g26400 | A06 | 18077507 | T | A | downstream_gene_variant | MODIFIER | c.*3722T>A| |
S168 |
19 | BAA06g26400 | A06 | 18077687 | C | T | downstream_gene_variant | MODIFIER | c.*3902C>T| |
S281 |
20 | BAA06g26400 | A06 | 18077892 | C | T | downstream_gene_variant | MODIFIER | c.*4107C>T| |
S77 S82 |
21 | BAA06g26400 | A06 | 18077925 | C | T | downstream_gene_variant | MODIFIER | c.*4140C>T| |
S264 |