Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18560 | A05 | 10678357 | C | T | upstream_gene_variant | MODIFIER | c.-4634C>T| |
S119 |
2 | BAA05g18560 | A05 | 10678423 | C | T | upstream_gene_variant | MODIFIER | c.-4568C>T| |
S180 |
3 | BAA05g18560 | A05 | 10678608 | G | A | upstream_gene_variant | MODIFIER | c.-4383G>A| |
S159 |
4 | BAA05g18560 | A05 | 10678741 | C | T | upstream_gene_variant | MODIFIER | c.-4250C>T| |
S103 |
5 | BAA05g18560 | A05 | 10678816 | T | C | upstream_gene_variant | MODIFIER | c.-4175T>C| |
S94 |
6 | BAA05g18560 | A05 | 10678906 | G | A | upstream_gene_variant | MODIFIER | c.-4085G>A| |
S138 |
7 | BAA05g18560 | A05 | 10679256 | G | A | upstream_gene_variant | MODIFIER | c.-3735G>A| |
S166 S167 S236 S257 |
8 | BAA05g18560 | A05 | 10679286 | G | A | upstream_gene_variant | MODIFIER | c.-3705G>A| |
S66 |
9 | BAA05g18560 | A05 | 10679378 | C | T | upstream_gene_variant | MODIFIER | c.-3613C>T| |
S261 |
10 | BAA05g18560 | A05 | 10679764 | C | T | upstream_gene_variant | MODIFIER | c.-3227C>T| |
S103 |
11 | BAA05g18560 | A05 | 10681098 | G | A | upstream_gene_variant | MODIFIER | c.-1893G>A| |
S297 |
12 | BAA05g18560 | A05 | 10681639 | G | A | upstream_gene_variant | MODIFIER | c.-1352G>A| |
S179 |
13 | BAA05g18560 | A05 | 10681708 | C | T | upstream_gene_variant | MODIFIER | c.-1283C>T| |
S57 |
14 | BAA05g18560 | A05 | 10682554 | G | A | upstream_gene_variant | MODIFIER | c.-437G>A| |
S245 |
15 | BAA05g18560 | A05 | 10683684 | A | G | missense_variant | MODERATE | c.551A>G|p.Asp184Gly |
S213 S228 S283 S292 S46 S8 S88 |
16 | BAA05g18560 | A05 | 10684397 | C | T | synonymous_variant | LOW | c.1264C>T|p.Leu422Leu |
S277 |
17 | BAA05g18560 | A05 | 10684638 | G | A | synonymous_variant | LOW | c.1413G>A|p.Lys471Lys |
S283 |
18 | BAA05g18560 | A05 | 10684918 | G | A | missense_variant | MODERATE | c.1693G>A|p.Asp565Asn |
S216 S265 |
19 | BAA05g18560 | A05 | 10686057 | G | A | missense_variant | MODERATE | c.2654G>A|p.Ser885Asn |
S115 |
20 | BAA05g18560 | A05 | 10686138 | T | A | missense_variant | MODERATE | c.2735T>A|p.Ile912Lys |
S166 |
21 | BAA05g18560 | A05 | 10686468 | G | A | missense_variant | MODERATE | c.2966G>A|p.Gly989Glu |
S238 |
22 | BAA05g18560 | A05 | 10686669 | G | A | downstream_gene_variant | MODIFIER | c.*65G>A| |
S264 |
23 | BAA05g18560 | A05 | 10687113 | G | A | downstream_gene_variant | MODIFIER | c.*509G>A| |
S159 |
24 | BAA05g18560 | A05 | 10687523 | T | C | downstream_gene_variant | MODIFIER | c.*919T>C| |
S206 |
25 | BAA05g18560 | A05 | 10687560 | G | A | downstream_gene_variant | MODIFIER | c.*956G>A| |
S149 |