Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26350 | A01 | 14663678 | G | A | missense_variant | MODERATE | c.2438C>T|p.Thr813Ile |
S245 |
2 | BAA01g26350 | A01 | 14663851 | C | T | intron_variant | MODIFIER | c.2335-70G>A| |
S183 |
3 | BAA01g26350 | A01 | 14664102 | G | A | synonymous_variant | LOW | c.2280C>T|p.Ser760Ser |
S14 |
4 | BAA01g26350 | A01 | 14666658 | G | A | synonymous_variant | LOW | c.753C>T|p.Phe251Phe |
S299 |
5 | BAA01g26350 | A01 | 14666990 | C | T | missense_variant | MODERATE | c.626G>A|p.Cys209Tyr |
S96 |
6 | BAA01g26350 | A01 | 14667840 | C | T | synonymous_variant | LOW | c.33G>A|p.Thr11Thr |
S296 |
7 | BAA01g26350 | A01 | 14667899 | C | T | upstream_gene_variant | MODIFIER | c.-27G>A| |
S150 |
8 | BAA01g26350 | A01 | 14667913 | C | T | upstream_gene_variant | MODIFIER | c.-41G>A| |
S177 |
9 | BAA01g26350 | A01 | 14667979 | C | T | upstream_gene_variant | MODIFIER | c.-107G>A| |
S182 |
10 | BAA01g26350 | A01 | 14668640 | G | A | upstream_gene_variant | MODIFIER | c.-768C>T| |
S1 S161 S90 |
11 | BAA01g26350 | A01 | 14668643 | G | A | upstream_gene_variant | MODIFIER | c.-771C>T| |
S187 |
12 | BAA01g26350 | A01 | 14669177 | C | T | upstream_gene_variant | MODIFIER | c.-1305G>A| |
S97 |
13 | BAA01g26350 | A01 | 14669436 | G | A | upstream_gene_variant | MODIFIER | c.-1564C>T| |
S110 |
14 | BAA01g26350 | A01 | 14669649 | G | A | upstream_gene_variant | MODIFIER | c.-1777C>T| |
S298 |
15 | BAA01g26350 | A01 | 14670249 | G | A | upstream_gene_variant | MODIFIER | c.-2377C>T| |
S236 |
16 | BAA01g26350 | A01 | 14670299 | C | T | upstream_gene_variant | MODIFIER | c.-2427G>A| |
S134 |