Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g17960 | A07 | 24094429 | G | A | intron_variant | MODIFIER | c.3690+25C>T| |
S48 |
2 | BAA07g17960 | A07 | 24094544 | G | A | intron_variant | MODIFIER | c.3622-22C>T| |
S291 |
3 | BAA07g17960 | A07 | 24096341 | C | T | intron_variant | MODIFIER | c.2848-41G>A| |
S8 |
4 | BAA07g17960 | A07 | 24096472 | C | T | synonymous_variant | LOW | c.2811G>A|p.Lys937Lys |
S162 |
5 | BAA07g17960 | A07 | 24097440 | G | A | splice_region_variant&intron_variant | LOW | c.2354-4C>T| |
S71 |
6 | BAA07g17960 | A07 | 24098826 | C | T | missense_variant | MODERATE | c.1549G>A|p.Gly517Arg |
S116 |
7 | BAA07g17960 | A07 | 24100003 | C | T | intron_variant | MODIFIER | c.946-37G>A| |
S161 |
8 | BAA07g17960 | A07 | 24100111 | G | A | synonymous_variant | LOW | c.879C>T|p.Ser293Ser |
S18 |
9 | BAA07g17960 | A07 | 24100582 | G | A | intron_variant | MODIFIER | c.530-17C>T| |
S183 |
10 | BAA07g17960 | A07 | 24100725 | G | A | missense_variant | MODERATE | c.479C>T|p.Ser160Leu |
S132 S137 S215 |
11 | BAA07g17960 | A07 | 24101374 | C | T | intron_variant | MODIFIER | c.261+117G>A| |
S42 |
12 | BAA07g17960 | A07 | 24101785 | G | A | synonymous_variant | LOW | c.93C>T|p.Ile31Ile |
S44 |
13 | BAA07g17960 | A07 | 24102165 | G | A | upstream_gene_variant | MODIFIER | c.-50C>T| |
S107 |
14 | BAA07g17960 | A07 | 24103427 | C | T | upstream_gene_variant | MODIFIER | c.-1312G>A| |
S249 |
15 | BAA07g17960 | A07 | 24104478 | C | T | upstream_gene_variant | MODIFIER | c.-2363G>A| |
S36 |