Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g25130 | A07 | 28053625 | C | T | downstream_gene_variant | MODIFIER | c.*1814G>A| |
S244 |
2 | BAA07g25130 | A07 | 28055702 | C | T | missense_variant | MODERATE | c.2452G>A|p.Asp818Asn |
S217 S248 |
3 | BAA07g25130 | A07 | 28055717 | C | T | missense_variant | MODERATE | c.2437G>A|p.Val813Met |
S177 |
4 | BAA07g25130 | A07 | 28056155 | G | A | synonymous_variant | LOW | c.1999C>T|p.Leu667Leu |
S295 |
5 | BAA07g25130 | A07 | 28056430 | C | T | missense_variant | MODERATE | c.1889G>A|p.Ser630Asn |
S136 |
6 | BAA07g25130 | A07 | 28057738 | G | A | missense_variant | MODERATE | c.1253C>T|p.Pro418Leu |
S299 |
7 | BAA07g25130 | A07 | 28058633 | G | A | synonymous_variant | LOW | c.465C>T|p.Asp155Asp |
S271 |
8 | BAA07g25130 | A07 | 28058845 | C | T | splice_region_variant&intron_variant | LOW | c.358+5G>A| |
S77 |
9 | BAA07g25130 | A07 | 28059406 | C | T | upstream_gene_variant | MODIFIER | c.-199G>A| |
S293 |
10 | BAA07g25130 | A07 | 28059846 | C | T | upstream_gene_variant | MODIFIER | c.-639G>A| |
S262 |
11 | BAA07g25130 | A07 | 28060416 | C | T | upstream_gene_variant | MODIFIER | c.-1209G>A| |
S1 S90 |
12 | BAA07g25130 | A07 | 28060803 | C | T | upstream_gene_variant | MODIFIER | c.-1596G>A| |
S62 |
13 | BAA07g25130 | A07 | 28061577 | C | T | upstream_gene_variant | MODIFIER | c.-2370G>A| |
S249 |
14 | BAA07g25130 | A07 | 28062388 | C | T | upstream_gene_variant | MODIFIER | c.-3181G>A| |
S299 |
15 | BAA07g25130 | A07 | 28062703 | C | T | upstream_gene_variant | MODIFIER | c.-3496G>A| |
S71 |
16 | BAA07g25130 | A07 | 28063237 | C | T | upstream_gene_variant | MODIFIER | c.-4030G>A| |
S34 |