Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g20800 | A06 | 11099564 | G | A | upstream_gene_variant | MODIFIER | c.-4219G>A| |
S228 |
2 | BAA06g20800 | A06 | 11101680 | C | T | upstream_gene_variant | MODIFIER | c.-2103C>T| |
S38 |
3 | BAA06g20800 | A06 | 11102210 | G | A | upstream_gene_variant | MODIFIER | c.-1573G>A| |
S20 |
4 | BAA06g20800 | A06 | 11102458 | G | A | upstream_gene_variant | MODIFIER | c.-1325G>A| |
S186 S275 |
5 | BAA06g20800 | A06 | 11103556 | C | T | upstream_gene_variant | MODIFIER | c.-227C>T| |
S239 |
6 | BAA06g20800 | A06 | 11105960 | C | T | intron_variant | MODIFIER | c.428-180C>T| |
S15 S3 |
7 | BAA06g20800 | A06 | 11105992 | G | A | intron_variant | MODIFIER | c.428-148G>A| |
S33 |
8 | BAA06g20800 | A06 | 11106133 | G | A | splice_region_variant&intron_variant | LOW | c.428-7G>A| |
S127 |
9 | BAA06g20800 | A06 | 11106781 | G | A | intron_variant | MODIFIER | c.828+120G>A| |
S81 S85 |
10 | BAA06g20800 | A06 | 11106831 | G | A | intron_variant | MODIFIER | c.828+170G>A| |
S13 |
11 | BAA06g20800 | A06 | 11107771 | G | A | intron_variant | MODIFIER | c.829-52G>A| |
S173 |
12 | BAA06g20800 | A06 | 11108466 | G | A | missense_variant | MODERATE | c.1024G>A|p.Glu342Lys |
S25 |
13 | BAA06g20800 | A06 | 11109240 | C | T | downstream_gene_variant | MODIFIER | c.*694C>T| |
S87 |
14 | BAA06g20800 | A06 | 11109251 | G | A | downstream_gene_variant | MODIFIER | c.*705G>A| |
S66 |
15 | BAA06g20800 | A06 | 11109774 | G | A | downstream_gene_variant | MODIFIER | c.*1228G>A| |
S126 |
16 | BAA06g20800 | A06 | 11109930 | G | A | downstream_gene_variant | MODIFIER | c.*1384G>A| |
S190 |
17 | BAA06g20800 | A06 | 11111105 | C | T | downstream_gene_variant | MODIFIER | c.*2559C>T| |
S174 |
18 | BAA06g20800 | A06 | 11112142 | C | T | downstream_gene_variant | MODIFIER | c.*3596C>T| |
S256 |