Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g49050 | A03 | 23543802 | G | A | intron_variant | MODIFIER | c.556-3729C>T| |
S167 |
2 | BAA03g49050 | A03 | 23544375 | C | T | intron_variant | MODIFIER | c.556-4302G>A| |
S216 |
3 | BAA03g49050 | A03 | 23544554 | C | T | intron_variant | MODIFIER | c.556-4481G>A| |
S244 |
4 | BAA03g49050 | A03 | 23544703 | G | A | intron_variant | MODIFIER | c.556-4630C>T| |
S114 |
5 | BAA03g49050 | A03 | 23544734 | C | T | intron_variant | MODIFIER | c.556-4661G>A| |
S225 S73 |
6 | BAA03g49050 | A03 | 23545018 | C | T | intron_variant | MODIFIER | c.556-4945G>A| |
S279 |
7 | BAA03g49050 | A03 | 23545487 | C | T | intron_variant | MODIFIER | c.556-5414G>A| |
S306 S308 |
8 | BAA03g49050 | A03 | 23545643 | C | T | intron_variant | MODIFIER | c.556-5570G>A| |
S281 |
9 | BAA03g49050 | A03 | 23545915 | C | T | intron_variant | MODIFIER | c.556-5842G>A| |
S45 |
10 | BAA03g49050 | A03 | 23546304 | T | C | intron_variant | MODIFIER | c.556-6231A>G| |
S279 |
11 | BAA03g49050 | A03 | 23551200 | C | T | intron_variant | MODIFIER | c.555+6638G>A| |
S293 |
12 | BAA03g49050 | A03 | 23551728 | G | A | intron_variant | MODIFIER | c.555+6110C>T| |
S69 |
13 | BAA03g49050 | A03 | 23552642 | G | A | intron_variant | MODIFIER | c.555+5196C>T| |
S109 |
14 | BAA03g49050 | A03 | 23554365 | C | T | intron_variant | MODIFIER | c.555+3473G>A| |
S126 |
15 | BAA03g49050 | A03 | 23554489 | C | T | intron_variant | MODIFIER | c.555+3349G>A| |
S279 |
16 | BAA03g49050 | A03 | 23554773 | C | T | intron_variant | MODIFIER | c.555+3065G>A| |
S42 |
17 | BAA03g49050 | A03 | 23554892 | G | A | intron_variant | MODIFIER | c.555+2946C>T| |
S233 |
18 | BAA03g49050 | A03 | 23554934 | C | T | intron_variant | MODIFIER | c.555+2904G>A| |
S120 |
19 | BAA03g49050 | A03 | 23555450 | C | T | intron_variant | MODIFIER | c.555+2388G>A| |
S117 |
20 | BAA03g49050 | A03 | 23555482 | C | T | intron_variant | MODIFIER | c.555+2356G>A| |
S92 |
21 | BAA03g49050 | A03 | 23555994 | G | A | intron_variant | MODIFIER | c.555+1844C>T| |
S292 |
22 | BAA03g49050 | A03 | 23556513 | G | A | intron_variant | MODIFIER | c.555+1325C>T| |
S284 |
23 | BAA03g49050 | A03 | 23557908 | G | A | missense_variant | MODERATE | c.485C>T|p.Pro162Leu |
S167 |
24 | BAA03g49050 | A03 | 23559418 | C | A | upstream_gene_variant | MODIFIER | c.-187G>T| |
S173 |
25 | BAA03g49050 | A03 | 23559479 | G | A | upstream_gene_variant | MODIFIER | c.-248C>T| |
S175 |