Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g10120 | A07 | 19007774 | C | T | synonymous_variant | LOW | c.2055G>A|p.Thr685Thr |
S236 |
2 | BAA07g10120 | A07 | 19008044 | C | T | synonymous_variant | LOW | c.1887G>A|p.Gln629Gln |
S85 |
3 | BAA07g10120 | A07 | 19008196 | G | A | stop_gained | HIGH | c.1735C>T|p.Gln579* |
S210 S225 |
4 | BAA07g10120 | A07 | 19009285 | C | T | synonymous_variant | LOW | c.1257G>A|p.Gln419Gln |
S19 |
5 | BAA07g10120 | A07 | 19009834 | G | A | missense_variant | MODERATE | c.802C>T|p.Pro268Ser |
S108 |
6 | BAA07g10120 | A07 | 19010154 | C | T | synonymous_variant | LOW | c.555G>A|p.Leu185Leu |
S155 S211 |
7 | BAA07g10120 | A07 | 19010369 | C | T | missense_variant | MODERATE | c.340G>A|p.Ala114Thr |
S23 |
8 | BAA07g10120 | A07 | 19010618 | C | T | missense_variant | MODERATE | c.91G>A|p.Val31Met |
S38 |
9 | BAA07g10120 | A07 | 19010740 | G | A | upstream_gene_variant | MODIFIER | c.-32C>T| |
S308 |
10 | BAA07g10120 | A07 | 19010858 | C | T | upstream_gene_variant | MODIFIER | c.-150G>A| |
S41 |
11 | BAA07g10120 | A07 | 19011431 | C | T | upstream_gene_variant | MODIFIER | c.-723G>A| |
S232 |
12 | BAA07g10120 | A07 | 19011752 | C | A | upstream_gene_variant | MODIFIER | c.-1044G>T| |
S8 |
13 | BAA07g10120 | A07 | 19012934 | C | T | upstream_gene_variant | MODIFIER | c.-2226G>A| |
S52 |
14 | BAA07g10120 | A07 | 19013006 | C | T | upstream_gene_variant | MODIFIER | c.-2298G>A| |
S191 |
15 | BAA07g10120 | A07 | 19013045 | C | T | upstream_gene_variant | MODIFIER | c.-2337G>A| |
S132 S137 S215 S288 S89 |
16 | BAA07g10120 | A07 | 19013683 | G | A | upstream_gene_variant | MODIFIER | c.-2975C>T| |
S269 |
17 | BAA07g10120 | A07 | 19014272 | G | A | upstream_gene_variant | MODIFIER | c.-3564C>T| |
S302 |