Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00490 | A02 | 268546 | C | T | upstream_gene_variant | MODIFIER | c.-4880C>T| |
S159 |
2 | BAA02g00490 | A02 | 268666 | G | A | upstream_gene_variant | MODIFIER | c.-4760G>A| |
S273 |
3 | BAA02g00490 | A02 | 269979 | C | T | upstream_gene_variant | MODIFIER | c.-3447C>T| |
S192 |
4 | BAA02g00490 | A02 | 270680 | C | T | upstream_gene_variant | MODIFIER | c.-2746C>T| |
S251 |
5 | BAA02g00490 | A02 | 270870 | C | T | upstream_gene_variant | MODIFIER | c.-2556C>T| |
S123 |
6 | BAA02g00490 | A02 | 273650 | G | A | synonymous_variant | LOW | c.153G>A|p.Glu51Glu |
S292 |
7 | BAA02g00490 | A02 | 273774 | G | A | missense_variant | MODERATE | c.277G>A|p.Glu93Lys |
S5 |
8 | BAA02g00490 | A02 | 273829 | G | A | missense_variant | MODERATE | c.332G>A|p.Gly111Asp |
S291 |
9 | BAA02g00490 | A02 | 274178 | C | T | synonymous_variant | LOW | c.681C>T|p.Leu227Leu |
S172 S217 |
10 | BAA02g00490 | A02 | 274878 | G | A | synonymous_variant | LOW | c.1245G>A|p.Glu415Glu |
S170 |
11 | BAA02g00490 | A02 | 275111 | G | A | missense_variant | MODERATE | c.1478G>A|p.Gly493Glu |
S78 S83 |
12 | BAA02g00490 | A02 | 275803 | C | T | missense_variant | MODERATE | c.2170C>T|p.Pro724Ser |
S218 |
13 | BAA02g00490 | A02 | 276554 | G | A | synonymous_variant | LOW | c.2493G>A|p.Gln831Gln |
S265 |
14 | BAA02g00490 | A02 | 276742 | G | A | missense_variant | MODERATE | c.2681G>A|p.Gly894Asp |
S259 |
15 | BAA02g00490 | A02 | 277100 | C | T | missense_variant | MODERATE | c.2957C>T|p.Ala986Val |
S207 |
16 | BAA02g00490 | A02 | 277370 | G | A | missense_variant | MODERATE | c.3227G>A|p.Gly1076Glu |
S107 |
17 | BAA02g00490 | A02 | 277436 | C | T | missense_variant | MODERATE | c.3293C>T|p.Pro1098Leu |
S142 |
18 | BAA02g00490 | A02 | 277850 | C | T | missense_variant | MODERATE | c.3515C>T|p.Ala1172Val |
S171 |
19 | BAA02g00490 | A02 | 279153 | C | T | synonymous_variant | LOW | c.4500C>T|p.Leu1500Leu |
S272 |
20 | BAA02g00490 | A02 | 279973 | G | A | missense_variant | MODERATE | c.5077G>A|p.Asp1693Asn |
S241 |
21 | BAA02g00490 | A02 | 280614 | C | T | missense_variant | MODERATE | c.5620C>T|p.Leu1874Phe |
S121 |
22 | BAA02g00490 | A02 | 280661 | G | A | splice_donor_variant&intron_variant | HIGH | c.5666+1G>A| |
S173 |