Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g19860 | A04 | 23183556 | C | T | missense_variant | MODERATE | c.3074G>A|p.Gly1025Glu |
S117 |
2 | BAA04g19860 | A04 | 23183577 | G | A | missense_variant | MODERATE | c.3053C>T|p.Ser1018Phe |
S129 |
3 | BAA04g19860 | A04 | 23183758 | G | A | synonymous_variant | LOW | c.2949C>T|p.Phe983Phe |
S174 S27 |
4 | BAA04g19860 | A04 | 23185695 | G | A | splice_region_variant&intron_variant | LOW | c.1848+4C>T| |
S71 |
5 | BAA04g19860 | A04 | 23186405 | G | A | missense_variant | MODERATE | c.1468C>T|p.Leu490Phe |
S281 |
6 | BAA04g19860 | A04 | 23186443 | C | T | missense_variant | MODERATE | c.1430G>A|p.Ser477Asn |
S65 |
7 | BAA04g19860 | A04 | 23186555 | C | T | synonymous_variant | LOW | c.1398G>A|p.Gln466Gln |
S74 |
8 | BAA04g19860 | A04 | 23189767 | G | A | splice_region_variant&intron_variant | LOW | c.16-5C>T| |
S162 |
9 | BAA04g19860 | A04 | 23190213 | C | T | upstream_gene_variant | MODIFIER | c.-342G>A| |
S187 |
10 | BAA04g19860 | A04 | 23190716 | G | A | upstream_gene_variant | MODIFIER | c.-845C>T| |
S288 |
11 | BAA04g19860 | A04 | 23193139 | G | A | upstream_gene_variant | MODIFIER | c.-3268C>T| |
S38 |
12 | BAA04g19860 | A04 | 23193183 | G | A | upstream_gene_variant | MODIFIER | c.-3312C>T| |
S40 S49 |
13 | BAA04g19860 | A04 | 23193638 | G | A | upstream_gene_variant | MODIFIER | c.-3767C>T| |
S218 |
14 | BAA04g19860 | A04 | 23194728 | C | T | upstream_gene_variant | MODIFIER | c.-4857G>A| |
S128 |