Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37210 | A02 | 31937437 | C | T | downstream_gene_variant | MODIFIER | c.*4180G>A| |
S212 |
2 | BAA02g37210 | A02 | 31938135 | C | T | downstream_gene_variant | MODIFIER | c.*3482G>A| |
S249 |
3 | BAA02g37210 | A02 | 31938775 | C | T | downstream_gene_variant | MODIFIER | c.*2842G>A| |
S239 |
4 | BAA02g37210 | A02 | 31938917 | A | C | downstream_gene_variant | MODIFIER | c.*2700T>G| |
S190 S286 |
5 | BAA02g37210 | A02 | 31939116 | G | A | downstream_gene_variant | MODIFIER | c.*2501C>T| |
S280 |
6 | BAA02g37210 | A02 | 31941012 | G | A | downstream_gene_variant | MODIFIER | c.*605C>T| |
S175 |
7 | BAA02g37210 | A02 | 31941667 | C | T | missense_variant | MODERATE | c.1822G>A|p.Ala608Thr |
S40 S49 |
8 | BAA02g37210 | A02 | 31942026 | C | T | missense_variant | MODERATE | c.1463G>A|p.Arg488Lys |
S116 S118 S148 S210 S30 S31 S54 |
9 | BAA02g37210 | A02 | 31942197 | C | T | missense_variant | MODERATE | c.1292G>A|p.Arg431Lys |
S119 |
10 | BAA02g37210 | A02 | 31943392 | C | T | synonymous_variant | LOW | c.162G>A|p.Glu54Glu |
S167 |
11 | BAA02g37210 | A02 | 31943996 | C | T | upstream_gene_variant | MODIFIER | c.-264G>A| |
S32 |
12 | BAA02g37210 | A02 | 31944320 | T | C | upstream_gene_variant | MODIFIER | c.-588A>G| |
S124 S126 S128 S129 S131 S190 S223 S25 S255 S264 S284 S286 S57 S60 S61 |
13 | BAA02g37210 | A02 | 31944961 | C | T | upstream_gene_variant | MODIFIER | c.-1229G>A| |
S231 |
14 | BAA02g37210 | A02 | 31946720 | G | A | upstream_gene_variant | MODIFIER | c.-2988C>T| |
S247 |
15 | BAA02g37210 | A02 | 31946864 | C | T | upstream_gene_variant | MODIFIER | c.-3132G>A| |
S63 |
16 | BAA02g37210 | A02 | 31946924 | C | T | upstream_gene_variant | MODIFIER | c.-3192G>A| |
S189 |
17 | BAA02g37210 | A02 | 31948567 | G | A | upstream_gene_variant | MODIFIER | c.-4835C>T| |
S169 |