Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g55640 | A03 | 27467603 | G | A | upstream_gene_variant | MODIFIER | c.-4954G>A| |
S169 |
2 | BAA03g55640 | A03 | 27467611 | G | A | upstream_gene_variant | MODIFIER | c.-4946G>A| |
S236 |
3 | BAA03g55640 | A03 | 27468040 | G | A | upstream_gene_variant | MODIFIER | c.-4517G>A| |
S210 S225 |
4 | BAA03g55640 | A03 | 27468607 | G | A | upstream_gene_variant | MODIFIER | c.-3950G>A| |
S280 |
5 | BAA03g55640 | A03 | 27471364 | G | A | upstream_gene_variant | MODIFIER | c.-1193G>A| |
S74 |
6 | BAA03g55640 | A03 | 27472200 | G | A | upstream_gene_variant | MODIFIER | c.-357G>A| |
S265 |
7 | BAA03g55640 | A03 | 27473861 | G | A | intron_variant | MODIFIER | c.1270+35G>A| |
S178 |
8 | BAA03g55640 | A03 | 27473876 | C | T | intron_variant | MODIFIER | c.1271-29C>T| |
S35 |
9 | BAA03g55640 | A03 | 27474131 | C | T | missense_variant | MODERATE | c.1415C>T|p.Thr472Ile |
S280 |
10 | BAA03g55640 | A03 | 27474601 | C | T | intron_variant | MODIFIER | c.1569+316C>T| |
S149 |
11 | BAA03g55640 | A03 | 27474761 | G | A | intron_variant | MODIFIER | c.1570-367G>A| |
S291 |
12 | BAA03g55640 | A03 | 27474902 | G | A | intron_variant | MODIFIER | c.1570-226G>A| |
S36 |
13 | BAA03g55640 | A03 | 27474998 | C | T | intron_variant | MODIFIER | c.1570-130C>T| |
S23 |