Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g15680 | A08 | 13193273 | G | A | upstream_gene_variant | MODIFIER | c.-4693G>A| |
S286 |
2 | BAA08g15680 | A08 | 13195202 | G | A | upstream_gene_variant | MODIFIER | c.-2764G>A| |
S232 |
3 | BAA08g15680 | A08 | 13195508 | C | T | upstream_gene_variant | MODIFIER | c.-2458C>T| |
S247 |
4 | BAA08g15680 | A08 | 13195953 | C | T | upstream_gene_variant | MODIFIER | c.-2013C>T| |
S292 |
5 | BAA08g15680 | A08 | 13197000 | G | A | upstream_gene_variant | MODIFIER | c.-966G>A| |
S107 |
6 | BAA08g15680 | A08 | 13199468 | C | T | intron_variant | MODIFIER | c.383+296C>T| |
S282 |
7 | BAA08g15680 | A08 | 13199944 | C | T | intron_variant | MODIFIER | c.383+772C>T| |
S233 |
8 | BAA08g15680 | A08 | 13200271 | C | T | intron_variant | MODIFIER | c.384-1044C>T| |
S171 |
9 | BAA08g15680 | A08 | 13200828 | C | T | intron_variant | MODIFIER | c.384-487C>T| |
S7 |
10 | BAA08g15680 | A08 | 13201346 | G | A | missense_variant | MODERATE | c.415G>A|p.Glu139Lys |
S53 |
11 | BAA08g15680 | A08 | 13201792 | C | T | intron_variant | MODIFIER | c.619+58C>T| |
S297 |
12 | BAA08g15680 | A08 | 13201887 | G | A | missense_variant | MODERATE | c.628G>A|p.Glu210Lys |
S232 |
13 | BAA08g15680 | A08 | 13202081 | C | T | downstream_gene_variant | MODIFIER | c.*5C>T| |
S148 S210 S31 |
14 | BAA08g15680 | A08 | 13203110 | G | A | downstream_gene_variant | MODIFIER | c.*1034G>A| |
S195 |
15 | BAA08g15680 | A08 | 13203532 | C | T | downstream_gene_variant | MODIFIER | c.*1456C>T| |
S305 |
16 | BAA08g15680 | A08 | 13203599 | G | A | downstream_gene_variant | MODIFIER | c.*1523G>A| |
S182 |
17 | BAA08g15680 | A08 | 13203921 | C | T | downstream_gene_variant | MODIFIER | c.*1845C>T| |
S157 S163 |
18 | BAA08g15680 | A08 | 13204006 | C | T | downstream_gene_variant | MODIFIER | c.*1930C>T| |
S156 |