Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g11270 | A04 | 17232548 | G | A | upstream_gene_variant | MODIFIER | c.-4682G>A| |
S274 |
2 | BAA04g11270 | A04 | 17233817 | C | T | upstream_gene_variant | MODIFIER | c.-3413C>T| |
S216 |
3 | BAA04g11270 | A04 | 17234096 | C | T | upstream_gene_variant | MODIFIER | c.-3134C>T| |
S186 S275 |
4 | BAA04g11270 | A04 | 17234391 | G | A | upstream_gene_variant | MODIFIER | c.-2839G>A| |
S190 |
5 | BAA04g11270 | A04 | 17235159 | G | A | upstream_gene_variant | MODIFIER | c.-2071G>A| |
S97 |
6 | BAA04g11270 | A04 | 17236377 | C | T | upstream_gene_variant | MODIFIER | c.-853C>T| |
S293 |
7 | BAA04g11270 | A04 | 17236817 | G | A | upstream_gene_variant | MODIFIER | c.-413G>A| |
S303 |
8 | BAA04g11270 | A04 | 17237125 | G | A | upstream_gene_variant | MODIFIER | c.-105G>A| |
S177 |
9 | BAA04g11270 | A04 | 17237282 | C | T | missense_variant | MODERATE | c.53C>T|p.Ser18Phe |
S98 |
10 | BAA04g11270 | A04 | 17238360 | C | T | synonymous_variant | LOW | c.1131C>T|p.His377His |
S296 |
11 | BAA04g11270 | A04 | 17238552 | G | A | missense_variant | MODERATE | c.1246G>A|p.Val416Ile |
S241 |
12 | BAA04g11270 | A04 | 17238621 | G | A | missense_variant | MODERATE | c.1315G>A|p.Asp439Asn |
S1 S228 S289 S290 S90 |
13 | BAA04g11270 | A04 | 17238774 | C | T | splice_region_variant&intron_variant | LOW | c.1389+8C>T| |
S136 |
14 | BAA04g11270 | A04 | 17239443 | G | A | missense_variant | MODERATE | c.1819G>A|p.Asp607Asn |
S12 |