Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g45490 | A06 | 29013952 | G | A | upstream_gene_variant | MODIFIER | c.-4695G>A| |
S171 |
2 | BAA06g45490 | A06 | 29015287 | G | A | upstream_gene_variant | MODIFIER | c.-3360G>A| |
S199 |
3 | BAA06g45490 | A06 | 29015365 | C | T | upstream_gene_variant | MODIFIER | c.-3282C>T| |
S68 |
4 | BAA06g45490 | A06 | 29016474 | C | T | upstream_gene_variant | MODIFIER | c.-2173C>T| |
S201 |
5 | BAA06g45490 | A06 | 29017465 | C | T | upstream_gene_variant | MODIFIER | c.-1182C>T| |
S236 |
6 | BAA06g45490 | A06 | 29018492 | C | T | upstream_gene_variant | MODIFIER | c.-155C>T| |
S184 |
7 | BAA06g45490 | A06 | 29019527 | G | A | missense_variant | MODERATE | c.428G>A|p.Gly143Glu |
S2 |
8 | BAA06g45490 | A06 | 29020001 | G | A | missense_variant | MODERATE | c.902G>A|p.Gly301Glu |
S140 |
9 | BAA06g45490 | A06 | 29020227 | C | T | synonymous_variant | LOW | c.1128C>T|p.Ile376Ile |
S293 |
10 | BAA06g45490 | A06 | 29020456 | G | A | missense_variant | MODERATE | c.1357G>A|p.Gly453Arg |
S292 |
11 | BAA06g45490 | A06 | 29020570 | G | A | missense_variant | MODERATE | c.1471G>A|p.Gly491Ser |
S158 |
12 | BAA06g45490 | A06 | 29023998 | G | A | downstream_gene_variant | MODIFIER | c.*3318G>A| |
S283 |