Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g13320 | A08 | 11553823 | G | A | upstream_gene_variant | MODIFIER | c.-4091G>A| |
S200 |
2 | BAA08g13320 | A08 | 11554066 | G | A | upstream_gene_variant | MODIFIER | c.-3848G>A| |
S5 |
3 | BAA08g13320 | A08 | 11554191 | C | T | upstream_gene_variant | MODIFIER | c.-3723C>T| |
S247 |
4 | BAA08g13320 | A08 | 11554428 | G | A | upstream_gene_variant | MODIFIER | c.-3486G>A| |
S13 |
5 | BAA08g13320 | A08 | 11555461 | G | A | upstream_gene_variant | MODIFIER | c.-2453G>A| |
S133 |
6 | BAA08g13320 | A08 | 11555493 | C | T | upstream_gene_variant | MODIFIER | c.-2421C>T| |
S171 |
7 | BAA08g13320 | A08 | 11555548 | C | T | upstream_gene_variant | MODIFIER | c.-2366C>T| |
S112 |
8 | BAA08g13320 | A08 | 11555608 | C | T | upstream_gene_variant | MODIFIER | c.-2306C>T| |
S169 |
9 | BAA08g13320 | A08 | 11555697 | C | T | upstream_gene_variant | MODIFIER | c.-2217C>T| |
S111 |
10 | BAA08g13320 | A08 | 11555954 | C | T | upstream_gene_variant | MODIFIER | c.-1960C>T| |
S210 S225 |
11 | BAA08g13320 | A08 | 11556071 | C | T | upstream_gene_variant | MODIFIER | c.-1843C>T| |
S209 |
12 | BAA08g13320 | A08 | 11556266 | C | T | upstream_gene_variant | MODIFIER | c.-1648C>T| |
S126 |
13 | BAA08g13320 | A08 | 11556856 | G | A | upstream_gene_variant | MODIFIER | c.-1058G>A| |
S260 |
14 | BAA08g13320 | A08 | 11557369 | C | T | upstream_gene_variant | MODIFIER | c.-545C>T| |
S142 |
15 | BAA08g13320 | A08 | 11557828 | C | T | upstream_gene_variant | MODIFIER | c.-86C>T| |
S71 |
16 | BAA08g13320 | A08 | 11557967 | G | A | synonymous_variant | LOW | c.54G>A|p.Glu18Glu |
S65 |
17 | BAA08g13320 | A08 | 11558247 | G | A | missense_variant&splice_region_variant | MODERATE | c.334G>A|p.Glu112Lys |
S65 |
18 | BAA08g13320 | A08 | 11558935 | G | A | intron_variant | MODIFIER | c.336+686G>A| |
S263 |
19 | BAA08g13320 | A08 | 11559176 | G | A | intron_variant | MODIFIER | c.337-833G>A| |
S103 |
20 | BAA08g13320 | A08 | 11559978 | C | T | intron_variant | MODIFIER | c.337-31C>T| |
S183 S198 |
21 | BAA08g13320 | A08 | 11560365 | G | A | missense_variant | MODERATE | c.553G>A|p.Val185Met |
S257 |