Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g04980 | A04 | 3148925 | G | A | downstream_gene_variant | MODIFIER | c.*821C>T| |
S144 |
2 | BAA04g04980 | A04 | 3149205 | C | A | downstream_gene_variant | MODIFIER | c.*541G>T| |
S23 |
3 | BAA04g04980 | A04 | 3149285 | C | T | downstream_gene_variant | MODIFIER | c.*461G>A| |
S172 S217 |
4 | BAA04g04980 | A04 | 3149413 | G | A | downstream_gene_variant | MODIFIER | c.*333C>T| |
S229 |
5 | BAA04g04980 | A04 | 3149872 | C | T | intron_variant | MODIFIER | c.185-29G>A| |
S130 S252 |
6 | BAA04g04980 | A04 | 3150024 | C | T | missense_variant | MODERATE | c.149G>A|p.Ser50Asn |
S1 S90 |
7 | BAA04g04980 | A04 | 3150859 | G | A | intron_variant | MODIFIER | c.37-723C>T| |
S87 |
8 | BAA04g04980 | A04 | 3150957 | G | A | intron_variant | MODIFIER | c.37-821C>T| |
S201 |
9 | BAA04g04980 | A04 | 3151122 | G | A | intron_variant | MODIFIER | c.37-986C>T| |
S264 |
10 | BAA04g04980 | A04 | 3151590 | C | T | intron_variant | MODIFIER | c.37-1454G>A| |
S82 S92 |
11 | BAA04g04980 | A04 | 3151867 | G | A | intron_variant | MODIFIER | c.37-1731C>T| |
S169 |
12 | BAA04g04980 | A04 | 3152238 | A | C | intron_variant | MODIFIER | c.36+1375T>G| |
S138 |
13 | BAA04g04980 | A04 | 3153151 | G | A | intron_variant | MODIFIER | c.36+462C>T| |
S10 |
14 | BAA04g04980 | A04 | 3153274 | G | A | intron_variant | MODIFIER | c.36+339C>T| |
S83 S88 |
15 | BAA04g04980 | A04 | 3153371 | G | A | intron_variant | MODIFIER | c.36+242C>T| |
S263 |
16 | BAA04g04980 | A04 | 3153840 | C | T | upstream_gene_variant | MODIFIER | c.-192G>A| |
S241 |
17 | BAA04g04980 | A04 | 3154077 | C | T | upstream_gene_variant | MODIFIER | c.-429G>A| |
S237 |
18 | BAA04g04980 | A04 | 3154367 | G | A | upstream_gene_variant | MODIFIER | c.-719C>T| |
S11 |
19 | BAA04g04980 | A04 | 3156359 | G | A | upstream_gene_variant | MODIFIER | c.-2711C>T| |
S136 |
20 | BAA04g04980 | A04 | 3157258 | G | A | upstream_gene_variant | MODIFIER | c.-3610C>T| |
S153 S213 |