Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g64090 | A03 | 33073955 | C | T | intron_variant | MODIFIER | c.1860-2430G>A| |
S277 |
2 | BAA03g64090 | A03 | 33074361 | G | A | intron_variant | MODIFIER | c.1860-2836C>T| |
S249 |
3 | BAA03g64090 | A03 | 33074771 | C | T | intron_variant | MODIFIER | c.1860-3246G>A| |
S13 |
4 | BAA03g64090 | A03 | 33075184 | G | A | intron_variant | MODIFIER | c.1860-3659C>T| |
S67 |
5 | BAA03g64090 | A03 | 33075380 | C | T | intron_variant | MODIFIER | c.1859+3523G>A| |
S292 |
6 | BAA03g64090 | A03 | 33075897 | C | T | intron_variant | MODIFIER | c.1859+3006G>A| |
S131 |
7 | BAA03g64090 | A03 | 33076708 | C | T | intron_variant | MODIFIER | c.1859+2195G>A| |
S292 |
8 | BAA03g64090 | A03 | 33077645 | G | A | intron_variant | MODIFIER | c.1859+1258C>T| |
S135 |
9 | BAA03g64090 | A03 | 33078191 | C | T | intron_variant | MODIFIER | c.1859+712G>A| |
S20 |
10 | BAA03g64090 | A03 | 33078493 | G | A | intron_variant | MODIFIER | c.1859+410C>T| |
S278 |
11 | BAA03g64090 | A03 | 33079066 | G | A | missense_variant | MODERATE | c.1696C>T|p.Pro566Ser |
S265 |
12 | BAA03g64090 | A03 | 33079265 | C | T | missense_variant | MODERATE | c.1585G>A|p.Ala529Thr |
S87 |
13 | BAA03g64090 | A03 | 33083017 | C | T | missense_variant | MODERATE | c.185G>A|p.Ser62Asn |
S161 |
14 | BAA03g64090 | A03 | 33084387 | C | T | upstream_gene_variant | MODIFIER | c.-457G>A| |
S113 |
15 | BAA03g64090 | A03 | 33084427 | G | A | upstream_gene_variant | MODIFIER | c.-497C>T| |
S284 |
16 | BAA03g64090 | A03 | 33085789 | C | T | upstream_gene_variant | MODIFIER | c.-1859G>A| |
S165 |
17 | BAA03g64090 | A03 | 33088206 | C | T | upstream_gene_variant | MODIFIER | c.-4276G>A| |
S2 S4 S6 |
18 | BAA03g64090 | A03 | 33088360 | C | T | upstream_gene_variant | MODIFIER | c.-4430G>A| |
S11 |