Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05610 | A10 | 2881489 | G | A | upstream_gene_variant | MODIFIER | c.-2729G>A| |
S274 |
2 | BAA10g05610 | A10 | 2881775 | C | T | upstream_gene_variant | MODIFIER | c.-2443C>T| |
S84 S93 |
3 | BAA10g05610 | A10 | 2883778 | C | T | upstream_gene_variant | MODIFIER | c.-440C>T| |
S155 S211 |
4 | BAA10g05610 | A10 | 2883922 | C | T | upstream_gene_variant | MODIFIER | c.-296C>T| |
S175 S177 |
5 | BAA10g05610 | A10 | 2884734 | G | A | missense_variant | MODERATE | c.211G>A|p.Gly71Arg |
S142 S65 |
6 | BAA10g05610 | A10 | 2885604 | C | T | missense_variant | MODERATE | c.739C>T|p.Arg247Cys |
S51 |
7 | BAA10g05610 | A10 | 2886209 | C | T | missense_variant | MODERATE | c.1228C>T|p.Pro410Ser |
S35 |
8 | BAA10g05610 | A10 | 2886455 | C | T | missense_variant | MODERATE | c.1474C>T|p.Leu492Phe |
S87 |
9 | BAA10g05610 | A10 | 2887105 | C | T | missense_variant | MODERATE | c.1763C>T|p.Pro588Leu |
S292 |
10 | BAA10g05610 | A10 | 2888996 | C | T | downstream_gene_variant | MODIFIER | c.*1848C>T| |
S229 |
11 | BAA10g05610 | A10 | 2889656 | G | A | downstream_gene_variant | MODIFIER | c.*2508G>A| |
S302 |