Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g38130 | A06 | 25020984 | G | A | upstream_gene_variant | MODIFIER | c.-3167G>A| |
S274 |
2 | BAA06g38130 | A06 | 25021494 | G | A | upstream_gene_variant | MODIFIER | c.-2657G>A| |
S218 |
3 | BAA06g38130 | A06 | 25021584 | C | T | upstream_gene_variant | MODIFIER | c.-2567C>T| |
S236 |
4 | BAA06g38130 | A06 | 25021782 | G | A | upstream_gene_variant | MODIFIER | c.-2369G>A| |
S12 |
5 | BAA06g38130 | A06 | 25022411 | C | T | upstream_gene_variant | MODIFIER | c.-1740C>T| |
S68 |
6 | BAA06g38130 | A06 | 25024610 | G | A | intron_variant | MODIFIER | c.310+51G>A| |
S23 |
7 | BAA06g38130 | A06 | 25024868 | C | T | missense_variant | MODERATE | c.370C>T|p.Leu124Phe |
S157 |
8 | BAA06g38130 | A06 | 25026489 | G | A | intron_variant | MODIFIER | c.1265-9G>A| |
S275 |
9 | BAA06g38130 | A06 | 25026917 | C | T | missense_variant | MODERATE | c.1684C>T|p.Leu562Phe |
S272 |
10 | BAA06g38130 | A06 | 25027809 | G | A | stop_gained | HIGH | c.2490G>A|p.Trp830* |
S139 |
11 | BAA06g38130 | A06 | 25027885 | C | T | intron_variant | MODIFIER | c.2550+16C>T| |
S69 |
12 | BAA06g38130 | A06 | 25030238 | C | T | missense_variant | MODERATE | c.3709C>T|p.Pro1237Ser |
S165 |
13 | BAA06g38130 | A06 | 25031092 | C | T | downstream_gene_variant | MODIFIER | c.*804C>T| |
S61 |
14 | BAA06g38130 | A06 | 25031203 | G | A | downstream_gene_variant | MODIFIER | c.*915G>A| |
S185 |
15 | BAA06g38130 | A06 | 25032357 | G | A | downstream_gene_variant | MODIFIER | c.*2069G>A| |
S105 |
16 | BAA06g38130 | A06 | 25033236 | G | A | downstream_gene_variant | MODIFIER | c.*2948G>A| |
S158 |