Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g02570 | A05 | 1393186 | C | T | missense_variant | MODERATE | c.2920G>A|p.Glu974Lys |
S20 |
2 | BAA05g02570 | A05 | 1393460 | C | T | missense_variant | MODERATE | c.2765G>A|p.Gly922Glu |
S107 |
3 | BAA05g02570 | A05 | 1395739 | G | A | missense_variant | MODERATE | c.1487C>T|p.Ala496Val |
S11 |
4 | BAA05g02570 | A05 | 1395905 | G | A | stop_gained | HIGH | c.1408C>T|p.Gln470* |
S175 S177 |
5 | BAA05g02570 | A05 | 1396092 | C | T | splice_region_variant&synonymous_variant | LOW | c.1299G>A|p.Lys433Lys |
S184 |
6 | BAA05g02570 | A05 | 1396304 | G | A | missense_variant | MODERATE | c.1087C>T|p.Leu363Phe |
S200 |
7 | BAA05g02570 | A05 | 1396344 | G | A | synonymous_variant | LOW | c.1047C>T|p.His349His |
S190 |
8 | BAA05g02570 | A05 | 1396385 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1007-1G>A| |
S140 |
9 | BAA05g02570 | A05 | 1396562 | G | A | missense_variant | MODERATE | c.908C>T|p.Ser303Phe |
S226 |
10 | BAA05g02570 | A05 | 1397163 | G | A | splice_region_variant&intron_variant | LOW | c.576+7C>T| |
S294 |
11 | BAA05g02570 | A05 | 1398332 | G | A | missense_variant | MODERATE | c.130C>T|p.Pro44Ser |
S184 |
12 | BAA05g02570 | A05 | 1398669 | G | A | upstream_gene_variant | MODIFIER | c.-208C>T| |
S16 |
13 | BAA05g02570 | A05 | 1398696 | G | A | upstream_gene_variant | MODIFIER | c.-235C>T| |
S226 |
14 | BAA05g02570 | A05 | 1400321 | C | T | upstream_gene_variant | MODIFIER | c.-1860G>A| |
S19 |
15 | BAA05g02570 | A05 | 1401193 | G | A | upstream_gene_variant | MODIFIER | c.-2732C>T| |
S289 |
16 | BAA05g02570 | A05 | 1402042 | G | A | upstream_gene_variant | MODIFIER | c.-3581C>T| |
S33 |
17 | BAA05g02570 | A05 | 1402624 | C | T | upstream_gene_variant | MODIFIER | c.-4163G>A| |
S271 |
18 | BAA05g02570 | A05 | 1402889 | C | T | upstream_gene_variant | MODIFIER | c.-4428G>A| |
S81 S85 |