Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22880 | A01 | 11611431 | C | T | upstream_gene_variant | MODIFIER | c.-2392C>T| |
S18 |
2 | BAA01g22880 | A01 | 11612689 | C | T | upstream_gene_variant | MODIFIER | c.-1134C>T| |
S19 |
3 | BAA01g22880 | A01 | 11612764 | G | A | upstream_gene_variant | MODIFIER | c.-1059G>A| |
S246 |
4 | BAA01g22880 | A01 | 11613347 | G | A | upstream_gene_variant | MODIFIER | c.-476G>A| |
S226 |
5 | BAA01g22880 | A01 | 11613424 | C | T | upstream_gene_variant | MODIFIER | c.-399C>T| |
S135 |
6 | BAA01g22880 | A01 | 11613760 | C | T | upstream_gene_variant | MODIFIER | c.-63C>T| |
S201 |
7 | BAA01g22880 | A01 | 11613789 | C | T | upstream_gene_variant | MODIFIER | c.-34C>T| |
S148 S30 S31 |
8 | BAA01g22880 | A01 | 11613830 | C | T | missense_variant | MODERATE | c.8C>T|p.Ser3Phe |
S282 |
9 | BAA01g22880 | A01 | 11614031 | G | A | missense_variant | MODERATE | c.209G>A|p.Arg70Lys |
S119 |
10 | BAA01g22880 | A01 | 11618111 | C | T | missense_variant | MODERATE | c.1148C>T|p.Thr383Ile |
S10 |
11 | BAA01g22880 | A01 | 11618378 | G | A | missense_variant | MODERATE | c.1415G>A|p.Arg472His |
S121 |
12 | BAA01g22880 | A01 | 11618459 | C | T | intron_variant | MODIFIER | c.1452+44C>T| |
S99 |
13 | BAA01g22880 | A01 | 11618658 | C | T | synonymous_variant | LOW | c.1485C>T|p.Val495Val |
S104 S52 |
14 | BAA01g22880 | A01 | 11618788 | G | A | missense_variant | MODERATE | c.1615G>A|p.Asp539Asn |
S292 |
15 | BAA01g22880 | A01 | 11619274 | G | A | intron_variant | MODIFIER | c.1854-18G>A| |
S59 |
16 | BAA01g22880 | A01 | 11619920 | C | T | missense_variant | MODERATE | c.2482C>T|p.Leu828Phe |
S179 |
17 | BAA01g22880 | A01 | 11622063 | G | A | missense_variant | MODERATE | c.3032G>A|p.Arg1011His |
S274 |
18 | BAA01g22880 | A01 | 11622393 | C | T | missense_variant | MODERATE | c.3362C>T|p.Ala1121Val |
S272 |
19 | BAA01g22880 | A01 | 11622897 | G | A | synonymous_variant | LOW | c.3783G>A|p.Leu1261Leu |
S280 |
20 | BAA01g22880 | A01 | 11623010 | C | T | missense_variant | MODERATE | c.3896C>T|p.Ser1299Phe |
S289 S290 |
21 | BAA01g22880 | A01 | 11623179 | G | A | missense_variant | MODERATE | c.3958G>A|p.Asp1320Asn |
S131 |
22 | BAA01g22880 | A01 | 11623852 | C | T | downstream_gene_variant | MODIFIER | c.*290C>T| |
S171 |
23 | BAA01g22880 | A01 | 11625262 | G | A | downstream_gene_variant | MODIFIER | c.*1700G>A| |
S56 |