Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g15250 | A07 | 22550249 | G | A | upstream_gene_variant | MODIFIER | c.-1453G>A| |
S175 |
2 | BAA07g15250 | A07 | 22550474 | G | A | upstream_gene_variant | MODIFIER | c.-1228G>A| |
S298 |
3 | BAA07g15250 | A07 | 22552181 | C | T | synonymous_variant | LOW | c.333C>T|p.Thr111Thr |
S162 |
4 | BAA07g15250 | A07 | 22553335 | G | A | synonymous_variant | LOW | c.1080G>A|p.Ala360Ala |
S115 |
5 | BAA07g15250 | A07 | 22553398 | C | T | intron_variant | MODIFIER | c.1125+18C>T| |
S169 |
6 | BAA07g15250 | A07 | 22553625 | C | T | synonymous_variant | LOW | c.1258C>T|p.Leu420Leu |
S294 |
7 | BAA07g15250 | A07 | 22553681 | C | T | synonymous_variant | LOW | c.1314C>T|p.Phe438Phe |
S168 |
8 | BAA07g15250 | A07 | 22554344 | C | T | synonymous_variant | LOW | c.1977C>T|p.Leu659Leu |
S200 |
9 | BAA07g15250 | A07 | 22554439 | C | T | missense_variant | MODERATE | c.2072C>T|p.Thr691Ile |
S143 |