Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g43250 | A05 | 40660683 | C | T | missense_variant | MODERATE | c.3809G>A|p.Gly1270Glu |
S209 |
2 | BAA05g43250 | A05 | 40660726 | C | T | missense_variant | MODERATE | c.3766G>A|p.Val1256Ile |
S226 |
3 | BAA05g43250 | A05 | 40660971 | C | T | missense_variant | MODERATE | c.3521G>A|p.Gly1174Glu |
S23 |
4 | BAA05g43250 | A05 | 40661352 | C | T | missense_variant | MODERATE | c.3224G>A|p.Gly1075Glu |
S260 |
5 | BAA05g43250 | A05 | 40662082 | G | A | intron_variant | MODIFIER | c.2677-15C>T| |
S70 |
6 | BAA05g43250 | A05 | 40662388 | C | T | missense_variant | MODERATE | c.2665G>A|p.Ala889Thr |
S200 |
7 | BAA05g43250 | A05 | 40663387 | C | T | missense_variant | MODERATE | c.1666G>A|p.Ala556Thr |
S244 |
8 | BAA05g43250 | A05 | 40663742 | C | T | synonymous_variant | LOW | c.1311G>A|p.Glu437Glu |
S192 |
9 | BAA05g43250 | A05 | 40663957 | C | T | missense_variant | MODERATE | c.1096G>A|p.Glu366Lys |
S294 |
10 | BAA05g43250 | A05 | 40663987 | C | T | missense_variant | MODERATE | c.1066G>A|p.Ala356Thr |
S293 |
11 | BAA05g43250 | A05 | 40666291 | C | T | missense_variant | MODERATE | c.55G>A|p.Glu19Lys |
S32 |
12 | BAA05g43250 | A05 | 40666303 | C | T | missense_variant | MODERATE | c.43G>A|p.Glu15Lys |
S223 |
13 | BAA05g43250 | A05 | 40666574 | C | T | upstream_gene_variant | MODIFIER | c.-229G>A| |
S86 |
14 | BAA05g43250 | A05 | 40666602 | C | T | upstream_gene_variant | MODIFIER | c.-257G>A| |
S206 S26 |
15 | BAA05g43250 | A05 | 40666764 | C | T | upstream_gene_variant | MODIFIER | c.-419G>A| |
S138 |
16 | BAA05g43250 | A05 | 40667056 | C | T | upstream_gene_variant | MODIFIER | c.-711G>A| |
S64 |
17 | BAA05g43250 | A05 | 40668686 | G | A | upstream_gene_variant | MODIFIER | c.-2341C>T| |
S261 |
18 | BAA05g43250 | A05 | 40668846 | G | A | upstream_gene_variant | MODIFIER | c.-2501C>T| |
S167 |
19 | BAA05g43250 | A05 | 40668890 | G | A | upstream_gene_variant | MODIFIER | c.-2545C>T| |
S261 |
20 | BAA05g43250 | A05 | 40671298 | G | A | upstream_gene_variant | MODIFIER | c.-4953C>T| |
S2 |