Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g05180 | A07 | 4459317 | C | T | intron_variant | MODIFIER | c.198-364C>T| |
S221 |
2 | BAA07g05180 | A07 | 4459335 | C | T | intron_variant | MODIFIER | c.198-346C>T| |
S58 |
3 | BAA07g05180 | A07 | 4459710 | C | T | missense_variant | MODERATE | c.227C>T|p.Thr76Ile |
S197 |
4 | BAA07g05180 | A07 | 4460454 | G | A | intron_variant | MODIFIER | c.400-265G>A| |
S240 |
5 | BAA07g05180 | A07 | 4461604 | C | T | downstream_gene_variant | MODIFIER | c.*134C>T| |
S173 |
6 | BAA07g05180 | A07 | 4463561 | C | T | downstream_gene_variant | MODIFIER | c.*2091C>T| |
S81 S85 |
7 | BAA07g05180 | A07 | 4464076 | G | A | downstream_gene_variant | MODIFIER | c.*2606G>A| |
S251 |
8 | BAA07g05180 | A07 | 4465461 | G | A | downstream_gene_variant | MODIFIER | c.*3991G>A| |
S223 |
9 | BAA07g05180 | A07 | 4465531 | C | T | downstream_gene_variant | MODIFIER | c.*4061C>T| |
S123 |
10 | BAA07g05180 | A07 | 4466148 | G | A | downstream_gene_variant | MODIFIER | c.*4678G>A| |
S10 |
11 | BAA07g05180 | A07 | 4466288 | C | T | downstream_gene_variant | MODIFIER | c.*4818C>T| |
S195 |