Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g29660 | A05 | 33083008 | C | T | upstream_gene_variant | MODIFIER | c.-3842C>T| |
S113 |
2 | BAA05g29660 | A05 | 33083755 | G | A | upstream_gene_variant | MODIFIER | c.-3095G>A| |
S178 |
3 | BAA05g29660 | A05 | 33083879 | G | A | upstream_gene_variant | MODIFIER | c.-2971G>A| |
S303 |
4 | BAA05g29660 | A05 | 33084594 | G | A | upstream_gene_variant | MODIFIER | c.-2256G>A| |
S219 S72 |
5 | BAA05g29660 | A05 | 33085033 | G | A | upstream_gene_variant | MODIFIER | c.-1817G>A| |
S6 |
6 | BAA05g29660 | A05 | 33085069 | G | A | upstream_gene_variant | MODIFIER | c.-1781G>A| |
S224 |
7 | BAA05g29660 | A05 | 33085914 | C | T | upstream_gene_variant | MODIFIER | c.-936C>T| |
S213 |
8 | BAA05g29660 | A05 | 33086276 | G | A | upstream_gene_variant | MODIFIER | c.-574G>A| |
S178 |
9 | BAA05g29660 | A05 | 33086411 | G | A | upstream_gene_variant | MODIFIER | c.-439G>A| |
S279 |
10 | BAA05g29660 | A05 | 33086531 | G | A | upstream_gene_variant | MODIFIER | c.-319G>A| |
S185 |
11 | BAA05g29660 | A05 | 33087500 | G | A | synonymous_variant | LOW | c.561G>A|p.Leu187Leu |
S257 |
12 | BAA05g29660 | A05 | 33088751 | C | T | intron_variant | MODIFIER | c.1003-40C>T| |
S207 |
13 | BAA05g29660 | A05 | 33089334 | G | A | intron_variant | MODIFIER | c.1179+367G>A| |
S156 |
14 | BAA05g29660 | A05 | 33092278 | C | T | intron_variant | MODIFIER | c.1179+3311C>T| |
S193 |
15 | BAA05g29660 | A05 | 33092937 | G | A | intron_variant | MODIFIER | c.1179+3970G>A| |
S165 |
16 | BAA05g29660 | A05 | 33096619 | C | T | intron_variant | MODIFIER | c.1180-292C>T| |
S288 |
17 | BAA05g29660 | A05 | 33097451 | G | A | synonymous_variant | LOW | c.1629G>A|p.Leu543Leu |
S308 |
18 | BAA05g29660 | A05 | 33097512 | C | T | missense_variant | MODERATE | c.1690C>T|p.Pro564Ser |
S139 |
19 | BAA05g29660 | A05 | 33097554 | C | T | missense_variant | MODERATE | c.1732C>T|p.Pro578Ser |
S12 |
20 | BAA05g29660 | A05 | 33097679 | G | A | synonymous_variant | LOW | c.1857G>A|p.Leu619Leu |
S185 |
21 | BAA05g29660 | A05 | 33103777 | C | T | downstream_gene_variant | MODIFIER | c.*3528C>T| |
S13 |
22 | BAA05g29660 | A05 | 33104344 | C | T | downstream_gene_variant | MODIFIER | c.*4095C>T| |
S286 |