Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15900 | A01 | 7731117 | C | T | upstream_gene_variant | MODIFIER | c.-4871C>T| |
S10 |
2 | BAA01g15900 | A01 | 7733501 | C | T | upstream_gene_variant | MODIFIER | c.-2487C>T| |
S226 |
3 | BAA01g15900 | A01 | 7734199 | C | T | upstream_gene_variant | MODIFIER | c.-1789C>T| |
S231 |
4 | BAA01g15900 | A01 | 7734423 | C | T | upstream_gene_variant | MODIFIER | c.-1565C>T| |
S182 |
5 | BAA01g15900 | A01 | 7735787 | C | T | upstream_gene_variant | MODIFIER | c.-201C>T| |
S286 |
6 | BAA01g15900 | A01 | 7736153 | G | A | intron_variant | MODIFIER | c.122-37G>A| |
S95 |
7 | BAA01g15900 | A01 | 7736671 | G | A | missense_variant | MODERATE | c.397G>A|p.Asp133Asn |
S173 |
8 | BAA01g15900 | A01 | 7736800 | C | T | intron_variant | MODIFIER | c.434-24C>T| |
S159 S243 |
9 | BAA01g15900 | A01 | 7736915 | C | T | synonymous_variant | LOW | c.525C>T|p.Ser175Ser |
S136 |
10 | BAA01g15900 | A01 | 7737193 | G | A | intron_variant | MODIFIER | c.591-147G>A| |
S72 S78 |
11 | BAA01g15900 | A01 | 7737706 | C | T | intron_variant | MODIFIER | c.673-100C>T| |
S169 |
12 | BAA01g15900 | A01 | 7738940 | G | A | intron_variant | MODIFIER | c.957+608G>A| |
S301 S304 |
13 | BAA01g15900 | A01 | 7739165 | G | A | intron_variant | MODIFIER | c.957+833G>A| |
S156 |
14 | BAA01g15900 | A01 | 7739444 | G | A | intron_variant | MODIFIER | c.957+1112G>A| |
S262 |
15 | BAA01g15900 | A01 | 7740006 | C | T | intron_variant | MODIFIER | c.957+1674C>T| |
S16 |
16 | BAA01g15900 | A01 | 7740604 | C | T | intron_variant | MODIFIER | c.957+2272C>T| |
S25 |
17 | BAA01g15900 | A01 | 7742720 | C | T | intron_variant | MODIFIER | c.958-1908C>T| |
S159 S243 |
18 | BAA01g15900 | A01 | 7743550 | C | T | intron_variant | MODIFIER | c.958-1078C>T| |
S303 |
19 | BAA01g15900 | A01 | 7743749 | C | T | intron_variant | MODIFIER | c.958-879C>T| |
S130 |
20 | BAA01g15900 | A01 | 7745137 | C | T | missense_variant | MODERATE | c.1094C>T|p.Ser365Leu |
S166 |
21 | BAA01g15900 | A01 | 7745357 | G | A | synonymous_variant | LOW | c.1314G>A|p.Lys438Lys |
S178 |
22 | BAA01g15900 | A01 | 7745456 | C | T | synonymous_variant | LOW | c.1413C>T|p.His471His |
S153 |
23 | BAA01g15900 | A01 | 7745695 | C | T | missense_variant | MODERATE | c.1652C>T|p.Thr551Ile |
S98 |
24 | BAA01g15900 | A01 | 7746253 | C | T | downstream_gene_variant | MODIFIER | c.*182C>T| |
S44 |