Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g01780 | A06 | 1112840 | C | T | upstream_gene_variant | MODIFIER | c.-4491C>T| |
S82 |
2 | BAA06g01780 | A06 | 1112970 | A | T | upstream_gene_variant | MODIFIER | c.-4361A>T| |
S193 |
3 | BAA06g01780 | A06 | 1113100 | C | T | upstream_gene_variant | MODIFIER | c.-4231C>T| |
S247 |
4 | BAA06g01780 | A06 | 1113644 | C | T | upstream_gene_variant | MODIFIER | c.-3687C>T| |
S192 |
5 | BAA06g01780 | A06 | 1113768 | G | A | upstream_gene_variant | MODIFIER | c.-3563G>A| |
S204 |
6 | BAA06g01780 | A06 | 1114765 | G | A | upstream_gene_variant | MODIFIER | c.-2566G>A| |
S113 |
7 | BAA06g01780 | A06 | 1115738 | C | T | upstream_gene_variant | MODIFIER | c.-1593C>T| |
S240 |
8 | BAA06g01780 | A06 | 1117384 | C | T | synonymous_variant | LOW | c.54C>T|p.Phe18Phe |
S13 |
9 | BAA06g01780 | A06 | 1117493 | G | A | missense_variant | MODERATE | c.163G>A|p.Asp55Asn |
S140 |
10 | BAA06g01780 | A06 | 1117575 | C | T | intron_variant | MODIFIER | c.182-22C>T| |
S221 |
11 | BAA06g01780 | A06 | 1117953 | C | T | intron_variant | MODIFIER | c.450+88C>T| |
S32 |
12 | BAA06g01780 | A06 | 1118452 | G | A | synonymous_variant | LOW | c.639G>A|p.Gln213Gln |
S149 |
13 | BAA06g01780 | A06 | 1118487 | C | T | missense_variant | MODERATE | c.674C>T|p.Pro225Leu |
S184 |
14 | BAA06g01780 | A06 | 1119214 | C | T | downstream_gene_variant | MODIFIER | c.*453C>T| |
S247 |
15 | BAA06g01780 | A06 | 1119566 | G | A | downstream_gene_variant | MODIFIER | c.*805G>A| |
S161 |
16 | BAA06g01780 | A06 | 1119768 | C | T | downstream_gene_variant | MODIFIER | c.*1007C>T| |
S274 |
17 | BAA06g01780 | A06 | 1120420 | C | T | downstream_gene_variant | MODIFIER | c.*1659C>T| |
S185 |
18 | BAA06g01780 | A06 | 1120753 | G | A | downstream_gene_variant | MODIFIER | c.*1992G>A| |
S81 S85 |
19 | BAA06g01780 | A06 | 1120998 | G | A | downstream_gene_variant | MODIFIER | c.*2237G>A| |
S179 |