Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g26690 | A06 | 18274999 | G | A | upstream_gene_variant | MODIFIER | c.-4660G>A| |
S230 |
2 | BAA06g26690 | A06 | 18275510 | C | T | upstream_gene_variant | MODIFIER | c.-4149C>T| |
S181 |
3 | BAA06g26690 | A06 | 18275920 | C | T | upstream_gene_variant | MODIFIER | c.-3739C>T| |
S64 |
4 | BAA06g26690 | A06 | 18276386 | T | C | upstream_gene_variant | MODIFIER | c.-3273T>C| |
S51 |
5 | BAA06g26690 | A06 | 18278250 | C | T | upstream_gene_variant | MODIFIER | c.-1409C>T| |
S111 |
6 | BAA06g26690 | A06 | 18278793 | C | T | upstream_gene_variant | MODIFIER | c.-866C>T| |
S79 S91 |
7 | BAA06g26690 | A06 | 18279623 | C | T | upstream_gene_variant | MODIFIER | c.-36C>T| |
S165 |
8 | BAA06g26690 | A06 | 18279701 | C | T | missense_variant | MODERATE | c.43C>T|p.Leu15Phe |
S280 |
9 | BAA06g26690 | A06 | 18279819 | C | G | intron_variant | MODIFIER | c.58-22C>G| |
S32 |
10 | BAA06g26690 | A06 | 18280649 | G | A | downstream_gene_variant | MODIFIER | c.*8G>A| |
S295 |
11 | BAA06g26690 | A06 | 18281198 | C | T | downstream_gene_variant | MODIFIER | c.*557C>T| |
S302 |
12 | BAA06g26690 | A06 | 18281213 | G | A | downstream_gene_variant | MODIFIER | c.*572G>A| |
S247 |
13 | BAA06g26690 | A06 | 18281333 | G | A | downstream_gene_variant | MODIFIER | c.*692G>A| |
S219 |
14 | BAA06g26690 | A06 | 18281918 | T | G | downstream_gene_variant | MODIFIER | c.*1277T>G| |
S109 S126 S127 S166 S279 |
15 | BAA06g26690 | A06 | 18282379 | C | T | downstream_gene_variant | MODIFIER | c.*1738C>T| |
S297 |
16 | BAA06g26690 | A06 | 18284854 | G | A | downstream_gene_variant | MODIFIER | c.*4213G>A| |
S89 |
17 | BAA06g26690 | A06 | 18284956 | G | A | downstream_gene_variant | MODIFIER | c.*4315G>A| |
S271 |
18 | BAA06g26690 | A06 | 18285417 | G | A | downstream_gene_variant | MODIFIER | c.*4776G>A| |
S74 |