Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g32300 | A02 | 27188448 | G | A | downstream_gene_variant | MODIFIER | c.*3171C>T| |
S279 |
2 | BAA02g32300 | A02 | 27188491 | G | A | downstream_gene_variant | MODIFIER | c.*3128C>T| |
S34 |
3 | BAA02g32300 | A02 | 27190927 | G | A | downstream_gene_variant | MODIFIER | c.*692C>T| |
S136 S247 |
4 | BAA02g32300 | A02 | 27191084 | C | T | downstream_gene_variant | MODIFIER | c.*535G>A| |
S64 |
5 | BAA02g32300 | A02 | 27191629 | G | A | missense_variant | MODERATE | c.3152C>T|p.Thr1051Ile |
S35 |
6 | BAA02g32300 | A02 | 27191858 | C | T | missense_variant | MODERATE | c.2923G>A|p.Glu975Lys |
S131 |
7 | BAA02g32300 | A02 | 27192225 | C | T | missense_variant | MODERATE | c.2635G>A|p.Glu879Lys |
S231 |
8 | BAA02g32300 | A02 | 27192363 | C | T | splice_region_variant&synonymous_variant | LOW | c.2592G>A|p.Leu864Leu |
S162 |
9 | BAA02g32300 | A02 | 27192492 | G | A | synonymous_variant | LOW | c.2463C>T|p.Asp821Asp |
S95 |
10 | BAA02g32300 | A02 | 27193232 | C | T | missense_variant | MODERATE | c.1723G>A|p.Glu575Lys |
S112 |
11 | BAA02g32300 | A02 | 27194742 | G | A | intron_variant | MODIFIER | c.566-26C>T| |
S159 S243 |
12 | BAA02g32300 | A02 | 27194793 | C | T | splice_region_variant&intron_variant | LOW | c.565+5G>A| |
S6 |
13 | BAA02g32300 | A02 | 27194820 | C | T | synonymous_variant | LOW | c.543G>A|p.Glu181Glu |
S216 |
14 | BAA02g32300 | A02 | 27194942 | C | T | splice_region_variant&intron_variant | LOW | c.483+5G>A| |
S305 |
15 | BAA02g32300 | A02 | 27195665 | G | A | synonymous_variant | LOW | c.126C>T|p.Ile42Ile |
S230 |
16 | BAA02g32300 | A02 | 27196888 | C | T | upstream_gene_variant | MODIFIER | c.-1098G>A| |
S211 |
17 | BAA02g32300 | A02 | 27197913 | C | T | upstream_gene_variant | MODIFIER | c.-2123G>A| |
S139 |
18 | BAA02g32300 | A02 | 27198306 | G | A | upstream_gene_variant | MODIFIER | c.-2516C>T| |
S186 |
19 | BAA02g32300 | A02 | 27200631 | C | T | upstream_gene_variant | MODIFIER | c.-4841G>A| |
S44 |