Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g29490 | A01 | 18615615 | C | T | upstream_gene_variant | MODIFIER | c.-3805C>T| |
S51 |
2 | BAA01g29490 | A01 | 18618115 | G | A | upstream_gene_variant | MODIFIER | c.-1305G>A| |
S116 |
3 | BAA01g29490 | A01 | 18619379 | G | A | upstream_gene_variant | MODIFIER | c.-41G>A| |
S159 S243 |
4 | BAA01g29490 | A01 | 18619561 | G | A | missense_variant&splice_region_variant | MODERATE | c.142G>A|p.Val48Met |
S86 |
5 | BAA01g29490 | A01 | 18619671 | C | T | intron_variant | MODIFIER | c.144+108C>T| |
S279 S51 |
6 | BAA01g29490 | A01 | 18621159 | G | A | intron_variant | MODIFIER | c.926+30G>A| |
S306 S308 |
7 | BAA01g29490 | A01 | 18621721 | C | T | intron_variant | MODIFIER | c.1074+39C>T| |
S35 |
8 | BAA01g29490 | A01 | 18622042 | C | T | synonymous_variant | LOW | c.1116C>T|p.Phe372Phe |
S146 |
9 | BAA01g29490 | A01 | 18622133 | C | T | intron_variant | MODIFIER | c.1176+31C>T| |
S42 |
10 | BAA01g29490 | A01 | 18622237 | C | T | missense_variant | MODERATE | c.1219C>T|p.Pro407Ser |
S142 |
11 | BAA01g29490 | A01 | 18622548 | C | T | intron_variant | MODIFIER | c.1297-43C>T| |
S186 |
12 | BAA01g29490 | A01 | 18623898 | C | T | synonymous_variant | LOW | c.1807C>T|p.Leu603Leu |
S127 |
13 | BAA01g29490 | A01 | 18628291 | G | A | downstream_gene_variant | MODIFIER | c.*2258G>A| |
S144 |
14 | BAA01g29490 | A01 | 18628690 | G | A | downstream_gene_variant | MODIFIER | c.*2657G>A| |
S274 |