Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g17000 | A07 | 23514921 | G | A | upstream_gene_variant | MODIFIER | c.-3572G>A| |
S2 |
2 | BAA07g17000 | A07 | 23517840 | C | T | upstream_gene_variant | MODIFIER | c.-653C>T| |
S169 |
3 | BAA07g17000 | A07 | 23518055 | C | T | upstream_gene_variant | MODIFIER | c.-438C>T| |
S148 S30 |
4 | BAA07g17000 | A07 | 23518314 | G | A | upstream_gene_variant | MODIFIER | c.-179G>A| |
S308 |
5 | BAA07g17000 | A07 | 23518555 | C | T | synonymous_variant | LOW | c.63C>T|p.Asn21Asn |
S68 |
6 | BAA07g17000 | A07 | 23519127 | C | T | intron_variant | MODIFIER | c.569+66C>T| |
S294 |
7 | BAA07g17000 | A07 | 23519131 | G | A | intron_variant | MODIFIER | c.569+70G>A| |
S200 |
8 | BAA07g17000 | A07 | 23519571 | C | T | intron_variant | MODIFIER | c.569+510C>T| |
S198 |
9 | BAA07g17000 | A07 | 23519669 | C | T | intron_variant | MODIFIER | c.569+608C>T| |
S217 S248 |
10 | BAA07g17000 | A07 | 23520713 | C | T | intron_variant | MODIFIER | c.569+1652C>T| |
S275 |
11 | BAA07g17000 | A07 | 23521219 | G | A | intron_variant | MODIFIER | c.569+2158G>A| |
S171 |
12 | BAA07g17000 | A07 | 23521390 | G | A | intron_variant | MODIFIER | c.569+2329G>A| |
S119 |
13 | BAA07g17000 | A07 | 23522422 | G | A | intron_variant | MODIFIER | c.570-3211G>A| |
S244 |
14 | BAA07g17000 | A07 | 23525976 | G | A | missense_variant | MODERATE | c.826G>A|p.Glu276Lys |
S54 |