Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g01430 | A07 | 997074 | G | A | missense_variant | MODERATE | c.454G>A|p.Val152Ile |
S19 |
2 | BAA07g01430 | A07 | 997314 | C | T | intron_variant | MODIFIER | c.577+117C>T| |
S161 |
3 | BAA07g01430 | A07 | 997397 | G | A | intron_variant | MODIFIER | c.577+200G>A| |
S208 S93 |
4 | BAA07g01430 | A07 | 998502 | C | T | intron_variant | MODIFIER | c.705+358C>T| |
S113 |
5 | BAA07g01430 | A07 | 999013 | C | T | intron_variant | MODIFIER | c.706-588C>T| |
S148 |
6 | BAA07g01430 | A07 | 999015 | C | T | intron_variant | MODIFIER | c.706-586C>T| |
S128 |
7 | BAA07g01430 | A07 | 999749 | C | T | missense_variant | MODERATE | c.854C>T|p.Pro285Leu |
S32 |
8 | BAA07g01430 | A07 | 1003063 | G | A | downstream_gene_variant | MODIFIER | c.*1945G>A| |
S223 |
9 | BAA07g01430 | A07 | 1003196 | G | A | downstream_gene_variant | MODIFIER | c.*2078G>A| |
S107 |
10 | BAA07g01430 | A07 | 1003318 | C | T | downstream_gene_variant | MODIFIER | c.*2200C>T| |
S150 |
11 | BAA07g01430 | A07 | 1003739 | G | A | downstream_gene_variant | MODIFIER | c.*2621G>A| |
S39 |
12 | BAA07g01430 | A07 | 1004659 | G | A | downstream_gene_variant | MODIFIER | c.*3541G>A| |
S112 |
13 | BAA07g01430 | A07 | 1004906 | G | A | downstream_gene_variant | MODIFIER | c.*3788G>A| |
S122 |
14 | BAA07g01430 | A07 | 1005274 | G | A | downstream_gene_variant | MODIFIER | c.*4156G>A| |
S278 |
15 | BAA07g01430 | A07 | 1005546 | A | T | downstream_gene_variant | MODIFIER | c.*4428A>T| |
S271 |