Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29330 | A02 | 16767301 | C | T | missense_variant | MODERATE | c.1619G>A|p.Cys540Tyr |
S77 |
2 | BAA02g29330 | A02 | 16767447 | C | T | synonymous_variant | LOW | c.1473G>A|p.Ser491Ser |
S293 |
3 | BAA02g29330 | A02 | 16768378 | C | T | missense_variant | MODERATE | c.664G>A|p.Val222Met |
S240 |
4 | BAA02g29330 | A02 | 16771412 | C | T | intron_variant | MODIFIER | c.545-965G>A| |
S78 |
5 | BAA02g29330 | A02 | 16771420 | G | T | intron_variant | MODIFIER | c.545-973C>A| |
S129 |
6 | BAA02g29330 | A02 | 16772180 | C | T | intron_variant | MODIFIER | c.545-1733G>A| |
S53 |
7 | BAA02g29330 | A02 | 16772539 | G | A | intron_variant | MODIFIER | c.545-2092C>T| |
S125 |
8 | BAA02g29330 | A02 | 16773077 | C | T | intron_variant | MODIFIER | c.545-2630G>A| |
S201 |
9 | BAA02g29330 | A02 | 16774881 | C | T | intron_variant | MODIFIER | c.545-4434G>A| |
S18 |
10 | BAA02g29330 | A02 | 16775628 | G | A | intron_variant | MODIFIER | c.544+5139C>T| |
S34 |
11 | BAA02g29330 | A02 | 16776433 | G | A | intron_variant | MODIFIER | c.544+4334C>T| |
S161 |
12 | BAA02g29330 | A02 | 16776887 | C | T | intron_variant | MODIFIER | c.544+3880G>A| |
S1 S90 |
13 | BAA02g29330 | A02 | 16777729 | T | A | intron_variant | MODIFIER | c.544+3038A>T| |
S299 |
14 | BAA02g29330 | A02 | 16778062 | G | A | intron_variant | MODIFIER | c.544+2705C>T| |
S94 |
15 | BAA02g29330 | A02 | 16778441 | G | T | intron_variant | MODIFIER | c.544+2326C>A| |
S244 |
16 | BAA02g29330 | A02 | 16780754 | C | T | intron_variant | MODIFIER | c.544+13G>A| |
S177 |
17 | BAA02g29330 | A02 | 16780853 | G | A | missense_variant | MODERATE | c.458C>T|p.Ala153Val |
S200 |
18 | BAA02g29330 | A02 | 16780879 | C | T | synonymous_variant | LOW | c.432G>A|p.Glu144Glu |
S112 |
19 | BAA02g29330 | A02 | 16780984 | G | A | synonymous_variant | LOW | c.327C>T|p.Asn109Asn |
S210 |
20 | BAA02g29330 | A02 | 16781558 | C | T | intron_variant | MODIFIER | c.213-460G>A| |
S240 |
21 | BAA02g29330 | A02 | 16782239 | C | T | intron_variant | MODIFIER | c.212+56G>A| |
S262 |
22 | BAA02g29330 | A02 | 16783299 | G | A | upstream_gene_variant | MODIFIER | c.-793C>T| |
S232 |
23 | BAA02g29330 | A02 | 16783691 | C | T | upstream_gene_variant | MODIFIER | c.-1185G>A| |
S264 |
24 | BAA02g29330 | A02 | 16784255 | C | T | upstream_gene_variant | MODIFIER | c.-1749G>A| |
S15 |
25 | BAA02g29330 | A02 | 16784684 | G | A | upstream_gene_variant | MODIFIER | c.-2178C>T| |
S26 |