Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g19000 | A07 | 24859733 | G | A | upstream_gene_variant | MODIFIER | c.-4717G>A| |
S240 |
2 | BAA07g19000 | A07 | 24861246 | C | T | upstream_gene_variant | MODIFIER | c.-3204C>T| |
S23 |
3 | BAA07g19000 | A07 | 24861316 | C | T | upstream_gene_variant | MODIFIER | c.-3134C>T| |
S233 |
4 | BAA07g19000 | A07 | 24862274 | C | T | upstream_gene_variant | MODIFIER | c.-2176C>T| |
S35 |
5 | BAA07g19000 | A07 | 24862570 | G | A | upstream_gene_variant | MODIFIER | c.-1880G>A| |
S70 |
6 | BAA07g19000 | A07 | 24862665 | C | T | upstream_gene_variant | MODIFIER | c.-1785C>T| |
S32 |
7 | BAA07g19000 | A07 | 24864646 | G | A | intron_variant | MODIFIER | c.67-123G>A| |
S223 |
8 | BAA07g19000 | A07 | 24865465 | G | A | intron_variant | MODIFIER | c.398+52G>A| |
S73 S91 |
9 | BAA07g19000 | A07 | 24865580 | G | A | missense_variant | MODERATE | c.446G>A|p.Gly149Glu |
S12 |
10 | BAA07g19000 | A07 | 24865653 | C | T | synonymous_variant | LOW | c.519C>T|p.Ile173Ile |
S47 |
11 | BAA07g19000 | A07 | 24866125 | G | A | missense_variant | MODERATE | c.758G>A|p.Gly253Glu |
S255 |