Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09280 | A10 | 11274698 | G | A | downstream_gene_variant | MODIFIER | c.*1256C>T| |
S178 |
2 | BAA10g09280 | A10 | 11275482 | G | A | downstream_gene_variant | MODIFIER | c.*472C>T| |
S4 |
3 | BAA10g09280 | A10 | 11276243 | C | T | missense_variant | MODERATE | c.1717G>A|p.Ala573Thr |
S177 |
4 | BAA10g09280 | A10 | 11276400 | T | G | intron_variant | MODIFIER | c.1709+61A>C| |
S15 S3 |
5 | BAA10g09280 | A10 | 11277199 | C | T | missense_variant | MODERATE | c.1486G>A|p.Glu496Lys |
S194 |
6 | BAA10g09280 | A10 | 11277633 | G | A | intron_variant | MODIFIER | c.1173-37C>T| |
S279 |
7 | BAA10g09280 | A10 | 11278447 | G | A | missense_variant | MODERATE | c.962C>T|p.Thr321Ile |
S138 |
8 | BAA10g09280 | A10 | 11278548 | A | T | splice_region_variant&intron_variant | LOW | c.958+5T>A| |
S15 |
9 | BAA10g09280 | A10 | 11278889 | C | T | missense_variant | MODERATE | c.817G>A|p.Gly273Arg |
S38 |
10 | BAA10g09280 | A10 | 11279544 | C | T | intron_variant | MODIFIER | c.568+73G>A| |
S286 |
11 | BAA10g09280 | A10 | 11280233 | T | G | missense_variant | MODERATE | c.236A>C|p.Lys79Thr |
S15 S3 |
12 | BAA10g09280 | A10 | 11280467 | C | T | missense_variant | MODERATE | c.94G>A|p.Glu32Lys |
S162 |
13 | BAA10g09280 | A10 | 11280895 | C | T | upstream_gene_variant | MODIFIER | c.-200G>A| |
S270 |