Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g22860 | A05 | 27515912 | C | T | downstream_gene_variant | MODIFIER | c.*4595G>A| |
S193 |
2 | BAA05g22860 | A05 | 27515960 | C | T | downstream_gene_variant | MODIFIER | c.*4547G>A| |
S216 |
3 | BAA05g22860 | A05 | 27516087 | C | T | downstream_gene_variant | MODIFIER | c.*4420G>A| |
S84 S93 |
4 | BAA05g22860 | A05 | 27516379 | C | T | downstream_gene_variant | MODIFIER | c.*4128G>A| |
S115 S43 |
5 | BAA05g22860 | A05 | 27516617 | C | T | downstream_gene_variant | MODIFIER | c.*3890G>A| |
S281 |
6 | BAA05g22860 | A05 | 27516729 | C | T | downstream_gene_variant | MODIFIER | c.*3778G>A| |
S25 |
7 | BAA05g22860 | A05 | 27516957 | G | A | downstream_gene_variant | MODIFIER | c.*3550C>T| |
S292 |
8 | BAA05g22860 | A05 | 27517920 | C | T | downstream_gene_variant | MODIFIER | c.*2587G>A| |
S53 |
9 | BAA05g22860 | A05 | 27517956 | G | A | downstream_gene_variant | MODIFIER | c.*2551C>T| |
S264 |
10 | BAA05g22860 | A05 | 27518992 | G | A | downstream_gene_variant | MODIFIER | c.*1515C>T| |
S67 |
11 | BAA05g22860 | A05 | 27519150 | G | A | downstream_gene_variant | MODIFIER | c.*1357C>T| |
S133 |
12 | BAA05g22860 | A05 | 27519555 | G | A | downstream_gene_variant | MODIFIER | c.*952C>T| |
S188 |
13 | BAA05g22860 | A05 | 27519586 | G | A | downstream_gene_variant | MODIFIER | c.*921C>T| |
S270 |
14 | BAA05g22860 | A05 | 27519719 | G | A | downstream_gene_variant | MODIFIER | c.*788C>T| |
S298 |
15 | BAA05g22860 | A05 | 27519904 | C | T | downstream_gene_variant | MODIFIER | c.*603G>A| |
S277 |
16 | BAA05g22860 | A05 | 27520469 | C | T | downstream_gene_variant | MODIFIER | c.*38G>A| |
S274 |
17 | BAA05g22860 | A05 | 27520868 | C | T | missense_variant | MODERATE | c.1360G>A|p.Glu454Lys |
S32 |
18 | BAA05g22860 | A05 | 27521123 | C | T | stop_gained | HIGH | c.1218G>A|p.Trp406* |
S271 |
19 | BAA05g22860 | A05 | 27521459 | G | A | intron_variant | MODIFIER | c.1014+23C>T| |
S25 |
20 | BAA05g22860 | A05 | 27521532 | G | A | missense_variant | MODERATE | c.964C>T|p.Leu322Phe |
S131 |
21 | BAA05g22860 | A05 | 27521926 | C | T | synonymous_variant | LOW | c.570G>A|p.Lys190Lys |
S239 S33 |
22 | BAA05g22860 | A05 | 27522378 | C | T | missense_variant&splice_region_variant | MODERATE | c.299G>A|p.Arg100Lys |
S171 |
23 | BAA05g22860 | A05 | 27522458 | G | A | intron_variant | MODIFIER | c.230-11C>T| |
S126 |
24 | BAA05g22860 | A05 | 27523132 | C | T | upstream_gene_variant | MODIFIER | c.-231G>A| |
S132 S137 S215 S237 S89 |
25 | BAA05g22860 | A05 | 27524637 | G | A | upstream_gene_variant | MODIFIER | c.-1736C>T| |
S77 S82 |