Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g36390 | A01 | 24386707 | G | A | downstream_gene_variant | MODIFIER | c.*2967C>T| |
S226 |
2 | BAA01g36390 | A01 | 24386755 | C | T | downstream_gene_variant | MODIFIER | c.*2919G>A| |
S275 |
3 | BAA01g36390 | A01 | 24386776 | C | T | downstream_gene_variant | MODIFIER | c.*2898G>A| |
S107 |
4 | BAA01g36390 | A01 | 24388842 | G | A | downstream_gene_variant | MODIFIER | c.*832C>T| |
S246 |
5 | BAA01g36390 | A01 | 24389193 | G | A | downstream_gene_variant | MODIFIER | c.*481C>T| |
S244 |
6 | BAA01g36390 | A01 | 24389488 | G | A | downstream_gene_variant | MODIFIER | c.*186C>T| |
S181 |
7 | BAA01g36390 | A01 | 24389619 | C | T | downstream_gene_variant | MODIFIER | c.*55G>A| |
S256 |
8 | BAA01g36390 | A01 | 24390170 | G | A | missense_variant | MODERATE | c.1823C>T|p.Ala608Val |
S20 |
9 | BAA01g36390 | A01 | 24391086 | C | T | missense_variant | MODERATE | c.1429G>A|p.Gly477Ser |
S183 S198 |
10 | BAA01g36390 | A01 | 24391413 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1285-1G>A| |
S32 |
11 | BAA01g36390 | A01 | 24391543 | G | T | missense_variant | MODERATE | c.1251C>A|p.Asn417Lys |
S117 S124 S148 S172 S210 S286 S298 S8 |
12 | BAA01g36390 | A01 | 24391828 | C | T | missense_variant | MODERATE | c.1103G>A|p.Arg368Lys |
S39 |
13 | BAA01g36390 | A01 | 24391851 | C | T | synonymous_variant | LOW | c.1080G>A|p.Glu360Glu |
S120 |
14 | BAA01g36390 | A01 | 24393447 | C | T | missense_variant | MODERATE | c.322G>A|p.Glu108Lys |
S264 |
15 | BAA01g36390 | A01 | 24394043 | C | T | missense_variant | MODERATE | c.25G>A|p.Glu9Lys |
S208 |
16 | BAA01g36390 | A01 | 24396977 | C | T | upstream_gene_variant | MODIFIER | c.-2910G>A| |
S98 |
17 | BAA01g36390 | A01 | 24397540 | G | A | upstream_gene_variant | MODIFIER | c.-3473C>T| |
S199 |