Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g20090 | A06 | 10532886 | G | A | downstream_gene_variant | MODIFIER | c.*2935C>T| |
S208 S219 |
2 | BAA06g20090 | A06 | 10534981 | G | A | downstream_gene_variant | MODIFIER | c.*840C>T| |
S184 S240 S278 |
3 | BAA06g20090 | A06 | 10535504 | G | A | downstream_gene_variant | MODIFIER | c.*317C>T| |
S61 |
4 | BAA06g20090 | A06 | 10535832 | C | T | missense_variant | MODERATE | c.1069G>A|p.Asp357Asn |
S294 |
5 | BAA06g20090 | A06 | 10536206 | C | T | intron_variant | MODIFIER | c.819+20G>A| |
S87 |
6 | BAA06g20090 | A06 | 10536241 | G | A | synonymous_variant | LOW | c.804C>T|p.Phe268Phe |
S213 |
7 | BAA06g20090 | A06 | 10536482 | C | T | missense_variant | MODERATE | c.563G>A|p.Gly188Asp |
S87 |
8 | BAA06g20090 | A06 | 10536647 | G | A | intron_variant | MODIFIER | c.443-45C>T| |
S216 |
9 | BAA06g20090 | A06 | 10536739 | G | A | intron_variant | MODIFIER | c.443-137C>T| |
S225 S73 |
10 | BAA06g20090 | A06 | 10537726 | C | T | upstream_gene_variant | MODIFIER | c.-238G>A| |
S34 |
11 | BAA06g20090 | A06 | 10538220 | C | T | upstream_gene_variant | MODIFIER | c.-732G>A| |
S286 |
12 | BAA06g20090 | A06 | 10539194 | C | T | upstream_gene_variant | MODIFIER | c.-1706G>A| |
S96 |
13 | BAA06g20090 | A06 | 10540020 | C | T | upstream_gene_variant | MODIFIER | c.-2532G>A| |
S155 S211 |
14 | BAA06g20090 | A06 | 10540633 | C | T | upstream_gene_variant | MODIFIER | c.-3145G>A| |
S242 |