Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g12690 | A01 | 5987272 | G | A | upstream_gene_variant | MODIFIER | c.-4264G>A| |
S138 |
2 | BAA01g12690 | A01 | 5987387 | G | A | upstream_gene_variant | MODIFIER | c.-4149G>A| |
S293 |
3 | BAA01g12690 | A01 | 5987634 | G | A | upstream_gene_variant | MODIFIER | c.-3902G>A| |
S181 |
4 | BAA01g12690 | A01 | 5989010 | G | A | upstream_gene_variant | MODIFIER | c.-2526G>A| |
S280 |
5 | BAA01g12690 | A01 | 5989084 | G | A | upstream_gene_variant | MODIFIER | c.-2452G>A| |
S245 |
6 | BAA01g12690 | A01 | 5989722 | C | T | upstream_gene_variant | MODIFIER | c.-1814C>T| |
S35 |
7 | BAA01g12690 | A01 | 5990128 | G | A | upstream_gene_variant | MODIFIER | c.-1408G>A| |
S236 |
8 | BAA01g12690 | A01 | 5991523 | C | T | upstream_gene_variant | MODIFIER | c.-13C>T| |
S78 |
9 | BAA01g12690 | A01 | 5991741 | G | A | missense_variant | MODERATE | c.206G>A|p.Arg69His |
S133 |
10 | BAA01g12690 | A01 | 5991871 | G | A | synonymous_variant | LOW | c.336G>A|p.Lys112Lys |
S28 |
11 | BAA01g12690 | A01 | 5992485 | G | A | missense_variant | MODERATE | c.950G>A|p.Gly317Glu |
S257 |
12 | BAA01g12690 | A01 | 5992566 | C | T | missense_variant | MODERATE | c.1031C>T|p.Thr344Ile |
S289 S290 |
13 | BAA01g12690 | A01 | 5992665 | G | A | missense_variant | MODERATE | c.1130G>A|p.Gly377Glu |
S142 |
14 | BAA01g12690 | A01 | 5992874 | C | T | missense_variant | MODERATE | c.1339C>T|p.Pro447Ser |
S136 |
15 | BAA01g12690 | A01 | 5993592 | C | T | synonymous_variant | LOW | c.1671C>T|p.Ala557Ala |
S198 |
16 | BAA01g12690 | A01 | 5993691 | C | T | downstream_gene_variant | MODIFIER | c.*63C>T| |
S135 |
17 | BAA01g12690 | A01 | 5993707 | C | T | downstream_gene_variant | MODIFIER | c.*79C>T| |
S108 |
18 | BAA01g12690 | A01 | 5995252 | C | T | downstream_gene_variant | MODIFIER | c.*1624C>T| |
S140 |
19 | BAA01g12690 | A01 | 5995384 | C | T | downstream_gene_variant | MODIFIER | c.*1756C>T| |
S112 |
20 | BAA01g12690 | A01 | 5996754 | G | A | downstream_gene_variant | MODIFIER | c.*3126G>A| |
S203 |
21 | BAA01g12690 | A01 | 5997669 | C | T | downstream_gene_variant | MODIFIER | c.*4041C>T| |
S249 |
22 | BAA01g12690 | A01 | 5998505 | G | A | downstream_gene_variant | MODIFIER | c.*4877G>A| |
S272 |