Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g12470 | A07 | 20782360 | G | A | missense_variant | MODERATE | c.349C>T|p.Leu117Phe |
S6 |
2 | BAA07g12470 | A07 | 20783218 | G | A | missense_variant | MODERATE | c.209C>T|p.Ala70Val |
S240 |
3 | BAA07g12470 | A07 | 20784072 | G | A | intron_variant | MODIFIER | c.124+545C>T| |
S249 |
4 | BAA07g12470 | A07 | 20784190 | G | A | intron_variant | MODIFIER | c.124+427C>T| |
S67 |
5 | BAA07g12470 | A07 | 20784448 | G | A | intron_variant | MODIFIER | c.124+169C>T| |
S87 |
6 | BAA07g12470 | A07 | 20785763 | C | T | upstream_gene_variant | MODIFIER | c.-1023G>A| |
S36 |
7 | BAA07g12470 | A07 | 20787013 | G | A | upstream_gene_variant | MODIFIER | c.-2273C>T| |
S123 |
8 | BAA07g12470 | A07 | 20788303 | G | A | upstream_gene_variant | MODIFIER | c.-3563C>T| |
S73 S91 |
9 | BAA07g12470 | A07 | 20788462 | G | A | upstream_gene_variant | MODIFIER | c.-3722C>T| |
S40 S49 |
10 | BAA07g12470 | A07 | 20789105 | G | A | upstream_gene_variant | MODIFIER | c.-4365C>T| |
S124 |
11 | BAA07g12470 | A07 | 20789136 | C | T | upstream_gene_variant | MODIFIER | c.-4396G>A| |
S245 |