Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g27330 | A08 | 19262862 | G | A | upstream_gene_variant | MODIFIER | c.-4097G>A| |
S287 |
2 | BAA08g27330 | A08 | 19263963 | G | A | upstream_gene_variant | MODIFIER | c.-2996G>A| |
S251 |
3 | BAA08g27330 | A08 | 19264814 | C | T | upstream_gene_variant | MODIFIER | c.-2145C>T| |
S35 |
4 | BAA08g27330 | A08 | 19265490 | C | T | upstream_gene_variant | MODIFIER | c.-1469C>T| |
S294 |
5 | BAA08g27330 | A08 | 19265607 | C | T | upstream_gene_variant | MODIFIER | c.-1352C>T| |
S209 |
6 | BAA08g27330 | A08 | 19266023 | G | A | upstream_gene_variant | MODIFIER | c.-936G>A| |
S216 |
7 | BAA08g27330 | A08 | 19266827 | G | A | upstream_gene_variant | MODIFIER | c.-132G>A| |
S75 S81 |
8 | BAA08g27330 | A08 | 19267656 | C | T | missense_variant | MODERATE | c.313C>T|p.Pro105Ser |
S82 S92 |
9 | BAA08g27330 | A08 | 19268624 | C | T | missense_variant | MODERATE | c.812C>T|p.Thr271Ile |
S162 |
10 | BAA08g27330 | A08 | 19268818 | G | A | missense_variant | MODERATE | c.1006G>A|p.Val336Ile |
S251 |
11 | BAA08g27330 | A08 | 19271617 | G | A | downstream_gene_variant | MODIFIER | c.*2335G>A| |
S282 |
12 | BAA08g27330 | A08 | 19272865 | C | T | downstream_gene_variant | MODIFIER | c.*3583C>T| |
S19 |
13 | BAA08g27330 | A08 | 19273636 | C | T | downstream_gene_variant | MODIFIER | c.*4354C>T| |
S213 |