Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17940 | A05 | 10195818 | C | T | synonymous_variant | LOW | c.1866G>A|p.Lys622Lys |
S277 |
2 | BAA05g17940 | A05 | 10196746 | G | A | synonymous_variant | LOW | c.1329C>T|p.Ser443Ser |
S148 S210 |
3 | BAA05g17940 | A05 | 10197373 | C | T | splice_donor_variant&intron_variant | HIGH | c.971+1G>A| |
S181 |
4 | BAA05g17940 | A05 | 10197377 | G | A | missense_variant | MODERATE | c.968C>T|p.Thr323Ile |
S122 |
5 | BAA05g17940 | A05 | 10197490 | C | T | synonymous_variant | LOW | c.855G>A|p.Lys285Lys |
S71 |
6 | BAA05g17940 | A05 | 10197926 | G | A | splice_region_variant&intron_variant | LOW | c.694-8C>T| |
S156 |
7 | BAA05g17940 | A05 | 10199138 | C | T | splice_region_variant&intron_variant | LOW | c.304-6G>A| |
S287 |
8 | BAA05g17940 | A05 | 10199344 | G | A | splice_region_variant&intron_variant | LOW | c.181-3C>T| |
S293 |
9 | BAA05g17940 | A05 | 10201276 | G | A | upstream_gene_variant | MODIFIER | c.-1233C>T| |
S192 |
10 | BAA05g17940 | A05 | 10203214 | G | A | upstream_gene_variant | MODIFIER | c.-3171C>T| |
S262 |
11 | BAA05g17940 | A05 | 10203560 | G | A | upstream_gene_variant | MODIFIER | c.-3517C>T| |
S292 |
12 | BAA05g17940 | A05 | 10203813 | C | T | upstream_gene_variant | MODIFIER | c.-3770G>A| |
S36 |
13 | BAA05g17940 | A05 | 10204135 | G | A | upstream_gene_variant | MODIFIER | c.-4092C>T| |
S200 |
14 | BAA05g17940 | A05 | 10204344 | G | A | upstream_gene_variant | MODIFIER | c.-4301C>T| |
S109 S301 S304 |