Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g20660 | A04 | 23687238 | C | T | downstream_gene_variant | MODIFIER | c.*4758G>A| |
S138 |
2 | BAA04g20660 | A04 | 23687581 | G | A | downstream_gene_variant | MODIFIER | c.*4415C>T| |
S87 |
3 | BAA04g20660 | A04 | 23688053 | C | T | downstream_gene_variant | MODIFIER | c.*3943G>A| |
S216 S241 |
4 | BAA04g20660 | A04 | 23688342 | G | A | downstream_gene_variant | MODIFIER | c.*3654C>T| |
S165 |
5 | BAA04g20660 | A04 | 23688899 | G | A | downstream_gene_variant | MODIFIER | c.*3097C>T| |
S169 |
6 | BAA04g20660 | A04 | 23690075 | G | A | downstream_gene_variant | MODIFIER | c.*1921C>T| |
S153 |
7 | BAA04g20660 | A04 | 23690291 | G | A | downstream_gene_variant | MODIFIER | c.*1705C>T| |
S293 |
8 | BAA04g20660 | A04 | 23690980 | C | T | downstream_gene_variant | MODIFIER | c.*1016G>A| |
S132 S137 S215 S89 |
9 | BAA04g20660 | A04 | 23690981 | C | T | downstream_gene_variant | MODIFIER | c.*1015G>A| |
S138 |
10 | BAA04g20660 | A04 | 23692016 | C | T | missense_variant | MODERATE | c.2287G>A|p.Glu763Lys |
S128 S60 |
11 | BAA04g20660 | A04 | 23692029 | C | T | stop_gained | HIGH | c.2274G>A|p.Trp758* |
S180 |
12 | BAA04g20660 | A04 | 23692582 | C | T | splice_region_variant&intron_variant | LOW | c.1728-7G>A| |
S25 |
13 | BAA04g20660 | A04 | 23693219 | C | T | intron_variant | MODIFIER | c.1494-120G>A| |
S243 S299 |
14 | BAA04g20660 | A04 | 23696147 | G | A | missense_variant | MODERATE | c.332C>T|p.Ser111Phe |
S277 |
15 | BAA04g20660 | A04 | 23698036 | G | A | upstream_gene_variant | MODIFIER | c.-996C>T| |
S234 |
16 | BAA04g20660 | A04 | 23698225 | C | T | upstream_gene_variant | MODIFIER | c.-1185G>A| |
S189 |
17 | BAA04g20660 | A04 | 23699842 | C | T | upstream_gene_variant | MODIFIER | c.-2802G>A| |
S135 |