Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g24650 | A05 | 29660267 | G | A | upstream_gene_variant | MODIFIER | c.-4908G>A| |
S160 |
2 | BAA05g24650 | A05 | 29660293 | G | A | upstream_gene_variant | MODIFIER | c.-4882G>A| |
S296 |
3 | BAA05g24650 | A05 | 29660328 | C | T | upstream_gene_variant | MODIFIER | c.-4847C>T| |
S98 |
4 | BAA05g24650 | A05 | 29660489 | C | T | upstream_gene_variant | MODIFIER | c.-4686C>T| |
S181 |
5 | BAA05g24650 | A05 | 29660571 | G | A | upstream_gene_variant | MODIFIER | c.-4604G>A| |
S266 |
6 | BAA05g24650 | A05 | 29661282 | G | A | upstream_gene_variant | MODIFIER | c.-3893G>A| |
S48 |
7 | BAA05g24650 | A05 | 29661696 | G | A | upstream_gene_variant | MODIFIER | c.-3479G>A| |
S125 |
8 | BAA05g24650 | A05 | 29661802 | G | A | upstream_gene_variant | MODIFIER | c.-3373G>A| |
S54 |
9 | BAA05g24650 | A05 | 29664180 | G | T | upstream_gene_variant | MODIFIER | c.-995G>T| |
S153 S213 |
10 | BAA05g24650 | A05 | 29664300 | C | T | upstream_gene_variant | MODIFIER | c.-875C>T| |
S241 |
11 | BAA05g24650 | A05 | 29664750 | G | A | upstream_gene_variant | MODIFIER | c.-425G>A| |
S293 |
12 | BAA05g24650 | A05 | 29664854 | C | T | upstream_gene_variant | MODIFIER | c.-321C>T| |
S100 |
13 | BAA05g24650 | A05 | 29665622 | C | T | missense_variant | MODERATE | c.370C>T|p.Arg124Cys |
S92 |
14 | BAA05g24650 | A05 | 29665840 | C | T | synonymous_variant | LOW | c.588C>T|p.Asp196Asp |
S157 |
15 | BAA05g24650 | A05 | 29666446 | C | T | synonymous_variant | LOW | c.1194C>T|p.Ser398Ser |
S294 |
16 | BAA05g24650 | A05 | 29667417 | G | A | missense_variant | MODERATE | c.2165G>A|p.Arg722Lys |
S144 |
17 | BAA05g24650 | A05 | 29667881 | C | T | synonymous_variant | LOW | c.2629C>T|p.Leu877Leu |
S175 |
18 | BAA05g24650 | A05 | 29669089 | G | A | synonymous_variant | LOW | c.3837G>A|p.Glu1279Glu |
S246 |
19 | BAA05g24650 | A05 | 29669151 | C | T | missense_variant | MODERATE | c.3899C>T|p.Thr1300Ile |
S169 S61 |
20 | BAA05g24650 | A05 | 29669339 | C | T | splice_region_variant&intron_variant | LOW | c.4080+7C>T| |
S166 |
21 | BAA05g24650 | A05 | 29669487 | C | T | missense_variant | MODERATE | c.4127C>T|p.Thr1376Ile |
S207 |