Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00830 | A08 | 610974 | G | A | upstream_gene_variant | MODIFIER | c.-4888G>A| |
S266 |
2 | BAA08g00830 | A08 | 611465 | G | A | upstream_gene_variant | MODIFIER | c.-4397G>A| |
S38 |
3 | BAA08g00830 | A08 | 612025 | C | T | upstream_gene_variant | MODIFIER | c.-3837C>T| |
S110 |
4 | BAA08g00830 | A08 | 612173 | C | T | upstream_gene_variant | MODIFIER | c.-3689C>T| |
S148 S30 S31 |
5 | BAA08g00830 | A08 | 612770 | G | A | upstream_gene_variant | MODIFIER | c.-3092G>A| |
S146 |
6 | BAA08g00830 | A08 | 613114 | G | A | upstream_gene_variant | MODIFIER | c.-2748G>A| |
S5 |
7 | BAA08g00830 | A08 | 613549 | C | T | upstream_gene_variant | MODIFIER | c.-2313C>T| |
S50 |
8 | BAA08g00830 | A08 | 614033 | G | A | upstream_gene_variant | MODIFIER | c.-1829G>A| |
S87 |
9 | BAA08g00830 | A08 | 614205 | C | T | upstream_gene_variant | MODIFIER | c.-1657C>T| |
S230 |
10 | BAA08g00830 | A08 | 614402 | G | A | upstream_gene_variant | MODIFIER | c.-1460G>A| |
S301 S304 |
11 | BAA08g00830 | A08 | 615324 | C | A | upstream_gene_variant | MODIFIER | c.-538C>A| |
S183 S198 |
12 | BAA08g00830 | A08 | 615784 | C | T | upstream_gene_variant | MODIFIER | c.-78C>T| |
S209 |
13 | BAA08g00830 | A08 | 616189 | C | T | stop_gained | HIGH | c.328C>T|p.Gln110* |
S126 |
14 | BAA08g00830 | A08 | 616238 | G | A | missense_variant | MODERATE | c.377G>A|p.Gly126Glu |
S297 |
15 | BAA08g00830 | A08 | 616267 | C | T | missense_variant | MODERATE | c.406C>T|p.Leu136Phe |
S47 |
16 | BAA08g00830 | A08 | 617986 | G | A | downstream_gene_variant | MODIFIER | c.*1555G>A| |
S32 |