Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g33270 | A06 | 22498767 | G | A | missense_variant | MODERATE | c.272G>A|p.Arg91Lys |
S118 |
2 | BAA06g33270 | A06 | 22499543 | G | A | synonymous_variant | LOW | c.771G>A|p.Lys257Lys |
S11 |
3 | BAA06g33270 | A06 | 22500262 | C | T | intron_variant | MODIFIER | c.1202+17C>T| |
S156 |
4 | BAA06g33270 | A06 | 22501005 | G | A | missense_variant | MODERATE | c.1609G>A|p.Glu537Lys |
S32 |
5 | BAA06g33270 | A06 | 22501681 | G | A | missense_variant | MODERATE | c.1963G>A|p.Ala655Thr |
S122 |
6 | BAA06g33270 | A06 | 22501894 | C | T | synonymous_variant | LOW | c.2037C>T|p.Leu679Leu |
S303 |
7 | BAA06g33270 | A06 | 22501966 | G | A | synonymous_variant | LOW | c.2109G>A|p.Gly703Gly |
S149 |
8 | BAA06g33270 | A06 | 22502126 | G | A | synonymous_variant | LOW | c.2187G>A|p.Gly729Gly |
S218 |
9 | BAA06g33270 | A06 | 22502373 | G | A | missense_variant | MODERATE | c.2434G>A|p.Gly812Arg |
S173 S49 |
10 | BAA06g33270 | A06 | 22502610 | G | A | synonymous_variant | LOW | c.2589G>A|p.Lys863Lys |
S250 |
11 | BAA06g33270 | A06 | 22502955 | C | T | missense_variant | MODERATE | c.2756C>T|p.Ala919Val |
S111 |
12 | BAA06g33270 | A06 | 22504285 | G | A | splice_region_variant&intron_variant | LOW | c.3133-4G>A| |
S13 |
13 | BAA06g33270 | A06 | 22504713 | G | A | downstream_gene_variant | MODIFIER | c.*92G>A| |
S17 |
14 | BAA06g33270 | A06 | 22504751 | G | A | downstream_gene_variant | MODIFIER | c.*130G>A| |
S125 |
15 | BAA06g33270 | A06 | 22505144 | C | T | downstream_gene_variant | MODIFIER | c.*523C>T| |
S115 |