Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g30790 | A06 | 20967174 | G | A | downstream_gene_variant | MODIFIER | c.*569C>T| |
S38 |
2 | BAA06g30790 | A06 | 20967966 | G | A | missense_variant | MODERATE | c.2711C>T|p.Ser904Phe |
S256 |
3 | BAA06g30790 | A06 | 20968033 | G | A | stop_gained | HIGH | c.2644C>T|p.Gln882* |
S168 |
4 | BAA06g30790 | A06 | 20968521 | C | T | synonymous_variant | LOW | c.2316G>A|p.Thr772Thr |
S274 |
5 | BAA06g30790 | A06 | 20968962 | G | A | synonymous_variant | LOW | c.2013C>T|p.Phe671Phe |
S176 |
6 | BAA06g30790 | A06 | 20969766 | G | A | intron_variant | MODIFIER | c.1534+20C>T| |
S219 S72 |
7 | BAA06g30790 | A06 | 20971214 | G | A | missense_variant | MODERATE | c.472C>T|p.Leu158Phe |
S32 |
8 | BAA06g30790 | A06 | 20971249 | G | A | missense_variant | MODERATE | c.437C>T|p.Ala146Val |
S297 |
9 | BAA06g30790 | A06 | 20971804 | G | A | intron_variant | MODIFIER | c.163-19C>T| |
S69 |
10 | BAA06g30790 | A06 | 20973188 | G | A | intron_variant | MODIFIER | c.42+1104C>T| |
S69 |
11 | BAA06g30790 | A06 | 20974867 | C | T | upstream_gene_variant | MODIFIER | c.-534G>A| |
S294 |
12 | BAA06g30790 | A06 | 20975293 | C | T | upstream_gene_variant | MODIFIER | c.-960G>A| |
S182 |
13 | BAA06g30790 | A06 | 20976260 | G | A | upstream_gene_variant | MODIFIER | c.-1927C>T| |
S202 |
14 | BAA06g30790 | A06 | 20976314 | C | T | upstream_gene_variant | MODIFIER | c.-1981G>A| |
S25 |
15 | BAA06g30790 | A06 | 20976449 | C | T | upstream_gene_variant | MODIFIER | c.-2116G>A| |
S298 |
16 | BAA06g30790 | A06 | 20976987 | C | T | upstream_gene_variant | MODIFIER | c.-2654G>A| |
S6 |
17 | BAA06g30790 | A06 | 20977661 | T | A | upstream_gene_variant | MODIFIER | c.-3328A>T| |
S250 |
18 | BAA06g30790 | A06 | 20977943 | G | A | upstream_gene_variant | MODIFIER | c.-3610C>T| |
S198 |