Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07980 | A10 | 5074348 | G | A | upstream_gene_variant | MODIFIER | c.-4934G>A| |
S109 |
2 | BAA10g07980 | A10 | 5074434 | C | T | upstream_gene_variant | MODIFIER | c.-4848C>T| |
S63 |
3 | BAA10g07980 | A10 | 5078791 | G | A | upstream_gene_variant | MODIFIER | c.-491G>A| |
S69 |
4 | BAA10g07980 | A10 | 5080528 | C | T | splice_region_variant&intron_variant | LOW | c.885-4C>T| |
S195 |
5 | BAA10g07980 | A10 | 5080589 | G | A | synonymous_variant | LOW | c.942G>A|p.Arg314Arg |
S238 |
6 | BAA10g07980 | A10 | 5080997 | G | A | intron_variant | MODIFIER | c.1049+301G>A| |
S39 |
7 | BAA10g07980 | A10 | 5081845 | G | A | missense_variant | MODERATE | c.1505G>A|p.Arg502Lys |
S289 |
8 | BAA10g07980 | A10 | 5082474 | C | T | downstream_gene_variant | MODIFIER | c.*520C>T| |
S142 S19 |
9 | BAA10g07980 | A10 | 5082897 | C | T | downstream_gene_variant | MODIFIER | c.*943C>T| |
S40 S49 |
10 | BAA10g07980 | A10 | 5083489 | T | G | downstream_gene_variant | MODIFIER | c.*1535T>G| |
S77 |
11 | BAA10g07980 | A10 | 5084193 | G | A | downstream_gene_variant | MODIFIER | c.*2239G>A| |
S262 |
12 | BAA10g07980 | A10 | 5084318 | C | T | downstream_gene_variant | MODIFIER | c.*2364C>T| |
S246 |
13 | BAA10g07980 | A10 | 5086049 | G | A | downstream_gene_variant | MODIFIER | c.*4095G>A| |
S290 |
14 | BAA10g07980 | A10 | 5086398 | G | A | downstream_gene_variant | MODIFIER | c.*4444G>A| |
S128 |