Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g32750 | A02 | 27979948 | G | A | upstream_gene_variant | MODIFIER | c.-4793G>A| |
S122 |
2 | BAA02g32750 | A02 | 27980589 | C | T | upstream_gene_variant | MODIFIER | c.-4152C>T| |
S280 |
3 | BAA02g32750 | A02 | 27980769 | G | A | upstream_gene_variant | MODIFIER | c.-3972G>A| |
S188 |
4 | BAA02g32750 | A02 | 27981090 | C | T | upstream_gene_variant | MODIFIER | c.-3651C>T| |
S219 S72 |
5 | BAA02g32750 | A02 | 27981849 | C | T | upstream_gene_variant | MODIFIER | c.-2892C>T| |
S181 |
6 | BAA02g32750 | A02 | 27982085 | G | A | upstream_gene_variant | MODIFIER | c.-2656G>A| |
S232 |
7 | BAA02g32750 | A02 | 27982225 | G | A | upstream_gene_variant | MODIFIER | c.-2516G>A| |
S71 |
8 | BAA02g32750 | A02 | 27983495 | G | A | upstream_gene_variant | MODIFIER | c.-1246G>A| |
S257 |
9 | BAA02g32750 | A02 | 27983680 | G | A | upstream_gene_variant | MODIFIER | c.-1061G>A| |
S34 |
10 | BAA02g32750 | A02 | 27984604 | G | A | upstream_gene_variant | MODIFIER | c.-137G>A| |
S297 |
11 | BAA02g32750 | A02 | 27985085 | C | T | synonymous_variant | LOW | c.345C>T|p.Ala115Ala |
S19 |
12 | BAA02g32750 | A02 | 27985981 | C | T | missense_variant | MODERATE | c.1241C>T|p.Pro414Leu |
S289 S290 |
13 | BAA02g32750 | A02 | 27986259 | C | T | intron_variant | MODIFIER | c.1482+37C>T| |
S189 |
14 | BAA02g32750 | A02 | 27986331 | G | A | missense_variant | MODERATE | c.1489G>A|p.Glu497Lys |
S168 |
15 | BAA02g32750 | A02 | 27986352 | G | A | missense_variant | MODERATE | c.1510G>A|p.Gly504Ser |
S26 |
16 | BAA02g32750 | A02 | 27986670 | G | A | missense_variant | MODERATE | c.1828G>A|p.Asp610Asn |
S113 |
17 | BAA02g32750 | A02 | 27986834 | G | A | synonymous_variant | LOW | c.1992G>A|p.Ala664Ala |
S134 |
18 | BAA02g32750 | A02 | 27987131 | G | A | synonymous_variant | LOW | c.2289G>A|p.Ser763Ser |
S276 |
19 | BAA02g32750 | A02 | 27987198 | G | A | missense_variant | MODERATE | c.2356G>A|p.Asp786Asn |
S13 |
20 | BAA02g32750 | A02 | 27987299 | G | A | stop_gained | HIGH | c.2457G>A|p.Trp819* |
S247 |
21 | BAA02g32750 | A02 | 27987340 | G | A | missense_variant | MODERATE | c.2498G>A|p.Arg833Lys |
S89 |
22 | BAA02g32750 | A02 | 27987474 | G | A | missense_variant | MODERATE | c.2560G>A|p.Asp854Asn |
S298 |
23 | BAA02g32750 | A02 | 27987499 | C | T | missense_variant | MODERATE | c.2585C>T|p.Ser862Phe |
S118 |
24 | BAA02g32750 | A02 | 27987768 | C | A | intron_variant | MODIFIER | c.2760+94C>A| |
S150 |
25 | BAA02g32750 | A02 | 27987769 | C | T | intron_variant | MODIFIER | c.2760+95C>T| |
S150 |