Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g27440 | A01 | 15839290 | C | T | upstream_gene_variant | MODIFIER | c.-2140C>T| |
S206 S26 |
2 | BAA01g27440 | A01 | 15840098 | G | A | upstream_gene_variant | MODIFIER | c.-1332G>A| |
S15 S3 |
3 | BAA01g27440 | A01 | 15840125 | C | T | upstream_gene_variant | MODIFIER | c.-1305C>T| |
S303 |
4 | BAA01g27440 | A01 | 15840432 | C | T | upstream_gene_variant | MODIFIER | c.-998C>T| |
S286 |
5 | BAA01g27440 | A01 | 15841015 | G | A | upstream_gene_variant | MODIFIER | c.-415G>A| |
S97 |
6 | BAA01g27440 | A01 | 15841217 | C | T | upstream_gene_variant | MODIFIER | c.-213C>T| |
S272 |
7 | BAA01g27440 | A01 | 15841466 | G | A | missense_variant | MODERATE | c.37G>A|p.Asp13Asn |
S276 |
8 | BAA01g27440 | A01 | 15842358 | C | T | missense_variant | MODERATE | c.374C>T|p.Ala125Val |
S142 |
9 | BAA01g27440 | A01 | 15843278 | C | T | missense_variant | MODERATE | c.784C>T|p.Pro262Ser |
S266 |
10 | BAA01g27440 | A01 | 15844055 | G | A | intron_variant | MODIFIER | c.1021-52G>A| |
S163 |
11 | BAA01g27440 | A01 | 15844180 | C | T | missense_variant | MODERATE | c.1094C>T|p.Thr365Ile |
S81 S85 |
12 | BAA01g27440 | A01 | 15844788 | G | A | missense_variant | MODERATE | c.1171G>A|p.Ala391Thr |
S278 |
13 | BAA01g27440 | A01 | 15845247 | G | A | splice_region_variant&synonymous_variant | LOW | c.1395G>A|p.Gln465Gln |
S121 |
14 | BAA01g27440 | A01 | 15846597 | G | A | missense_variant | MODERATE | c.2080G>A|p.Ala694Thr |
S249 |
15 | BAA01g27440 | A01 | 15847085 | C | T | missense_variant | MODERATE | c.2228C>T|p.Ala743Val |
S85 |
16 | BAA01g27440 | A01 | 15848334 | C | T | missense_variant | MODERATE | c.2878C>T|p.Leu960Phe |
S198 |
17 | BAA01g27440 | A01 | 15849563 | G | A | downstream_gene_variant | MODIFIER | c.*958G>A| |
S38 |
18 | BAA01g27440 | A01 | 15849971 | G | A | downstream_gene_variant | MODIFIER | c.*1366G>A| |
S58 |