Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g15790 | A04 | 20457390 | C | T | upstream_gene_variant | MODIFIER | c.-4956C>T| |
S156 |
2 | BAA04g15790 | A04 | 20459650 | G | A | upstream_gene_variant | MODIFIER | c.-2696G>A| |
S303 |
3 | BAA04g15790 | A04 | 20459841 | G | A | upstream_gene_variant | MODIFIER | c.-2505G>A| |
S156 |
4 | BAA04g15790 | A04 | 20459896 | G | A | upstream_gene_variant | MODIFIER | c.-2450G>A| |
S71 |
5 | BAA04g15790 | A04 | 20460426 | C | T | upstream_gene_variant | MODIFIER | c.-1920C>T| |
S295 |
6 | BAA04g15790 | A04 | 20460718 | C | T | upstream_gene_variant | MODIFIER | c.-1628C>T| |
S294 |
7 | BAA04g15790 | A04 | 20460916 | C | T | upstream_gene_variant | MODIFIER | c.-1430C>T| |
S231 |
8 | BAA04g15790 | A04 | 20461074 | G | A | upstream_gene_variant | MODIFIER | c.-1272G>A| |
S164 |
9 | BAA04g15790 | A04 | 20461374 | G | A | upstream_gene_variant | MODIFIER | c.-972G>A| |
S12 |
10 | BAA04g15790 | A04 | 20461415 | G | A | upstream_gene_variant | MODIFIER | c.-931G>A| |
S124 |
11 | BAA04g15790 | A04 | 20461448 | G | A | upstream_gene_variant | MODIFIER | c.-898G>A| |
S85 |
12 | BAA04g15790 | A04 | 20462295 | A | T | upstream_gene_variant | MODIFIER | c.-51A>T| |
S150 |
13 | BAA04g15790 | A04 | 20462349 | G | A | missense_variant | MODERATE | c.4G>A|p.Asp2Asn |
S50 |
14 | BAA04g15790 | A04 | 20463416 | C | T | missense_variant | MODERATE | c.635C>T|p.Ala212Val |
S67 |
15 | BAA04g15790 | A04 | 20464714 | G | A | splice_donor_variant&intron_variant | HIGH | c.1598+1G>A| |
S38 |
16 | BAA04g15790 | A04 | 20465010 | G | A | synonymous_variant | LOW | c.1722G>A|p.Glu574Glu |
S175 |