Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g51020 | A03 | 24745751 | G | A | downstream_gene_variant | MODIFIER | c.*825C>T| |
S206 |
2 | BAA03g51020 | A03 | 24747323 | G | A | intron_variant | MODIFIER | c.973-66C>T| |
S262 |
3 | BAA03g51020 | A03 | 24747360 | G | A | intron_variant | MODIFIER | c.973-103C>T| |
S6 |
4 | BAA03g51020 | A03 | 24748479 | G | A | intron_variant | MODIFIER | c.973-1222C>T| |
S271 |
5 | BAA03g51020 | A03 | 24749326 | C | T | intron_variant | MODIFIER | c.972+1697G>A| |
S200 |
6 | BAA03g51020 | A03 | 24749460 | A | T | intron_variant | MODIFIER | c.972+1563T>A| |
S148 S210 S31 |
7 | BAA03g51020 | A03 | 24749622 | C | T | intron_variant | MODIFIER | c.972+1401G>A| |
S263 |
8 | BAA03g51020 | A03 | 24750605 | G | A | intron_variant | MODIFIER | c.972+418C>T| |
S146 |
9 | BAA03g51020 | A03 | 24751006 | G | A | intron_variant | MODIFIER | c.972+17C>T| |
S10 |
10 | BAA03g51020 | A03 | 24751179 | C | T | intron_variant | MODIFIER | c.831-15G>A| |
S117 |
11 | BAA03g51020 | A03 | 24751928 | G | A | missense_variant | MODERATE | c.281C>T|p.Ser94Phe |
S112 |
12 | BAA03g51020 | A03 | 24753043 | C | T | upstream_gene_variant | MODIFIER | c.-712G>A| |
S32 |
13 | BAA03g51020 | A03 | 24753427 | G | A | upstream_gene_variant | MODIFIER | c.-1096C>T| |
S1 |
14 | BAA03g51020 | A03 | 24756027 | G | A | upstream_gene_variant | MODIFIER | c.-3696C>T| |
S36 |
15 | BAA03g51020 | A03 | 24756167 | G | A | upstream_gene_variant | MODIFIER | c.-3836C>T| |
S191 |
16 | BAA03g51020 | A03 | 24756234 | G | A | upstream_gene_variant | MODIFIER | c.-3903C>T| |
S302 |
17 | BAA03g51020 | A03 | 24756297 | C | T | upstream_gene_variant | MODIFIER | c.-3966G>A| |
S15 S3 |