Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g28600 | A01 | 17922481 | C | T | synonymous_variant | LOW | c.792C>T|p.Cys264Cys |
S111 |
2 | BAA01g28600 | A01 | 17922527 | C | T | missense_variant | MODERATE | c.838C>T|p.Pro280Ser |
S269 |
3 | BAA01g28600 | A01 | 17927087 | C | T | intron_variant | MODIFIER | c.2569+27C>T| |
S282 |
4 | BAA01g28600 | A01 | 17927779 | C | T | intron_variant | MODIFIER | c.2811+54C>T| |
S13 S140 S168 S64 |
5 | BAA01g28600 | A01 | 17928389 | C | T | intron_variant | MODIFIER | c.3103+31C>T| |
S293 |
6 | BAA01g28600 | A01 | 17928772 | C | T | missense_variant | MODERATE | c.3350C>T|p.Ser1117Phe |
S284 |
7 | BAA01g28600 | A01 | 17928777 | G | A | missense_variant&splice_region_variant | MODERATE | c.3355G>A|p.Glu1119Lys |
S241 |
8 | BAA01g28600 | A01 | 17929499 | C | T | downstream_gene_variant | MODIFIER | c.*389C>T| |
S32 |
9 | BAA01g28600 | A01 | 17929830 | G | A | downstream_gene_variant | MODIFIER | c.*720G>A| |
S163 |
10 | BAA01g28600 | A01 | 17929994 | C | T | downstream_gene_variant | MODIFIER | c.*884C>T| |
S35 |
11 | BAA01g28600 | A01 | 17930146 | G | A | downstream_gene_variant | MODIFIER | c.*1036G>A| |
S280 |
12 | BAA01g28600 | A01 | 17930255 | G | A | downstream_gene_variant | MODIFIER | c.*1145G>A| |
S288 |
13 | BAA01g28600 | A01 | 17930795 | G | A | downstream_gene_variant | MODIFIER | c.*1685G>A| |
S61 |
14 | BAA01g28600 | A01 | 17930859 | G | A | downstream_gene_variant | MODIFIER | c.*1749G>A| |
S75 |