Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g38660 | A03 | 17915288 | G | A | upstream_gene_variant | MODIFIER | c.-3790G>A| |
S130 |
2 | BAA03g38660 | A03 | 17915708 | G | A | upstream_gene_variant | MODIFIER | c.-3370G>A| |
S48 |
3 | BAA03g38660 | A03 | 17915863 | G | A | upstream_gene_variant | MODIFIER | c.-3215G>A| |
S265 |
4 | BAA03g38660 | A03 | 17916938 | C | T | upstream_gene_variant | MODIFIER | c.-2140C>T| |
S210 S225 S241 |
5 | BAA03g38660 | A03 | 17917029 | T | C | upstream_gene_variant | MODIFIER | c.-2049T>C| |
S302 |
6 | BAA03g38660 | A03 | 17918197 | C | T | upstream_gene_variant | MODIFIER | c.-881C>T| |
S8 |
7 | BAA03g38660 | A03 | 17918863 | G | A | upstream_gene_variant | MODIFIER | c.-215G>A| |
S260 |
8 | BAA03g38660 | A03 | 17919239 | C | T | synonymous_variant | LOW | c.162C>T|p.Leu54Leu |
S85 |
9 | BAA03g38660 | A03 | 17919661 | G | A | missense_variant | MODERATE | c.331G>A|p.Asp111Asn |
S142 |
10 | BAA03g38660 | A03 | 17919920 | C | T | intron_variant | MODIFIER | c.498+92C>T| |
S62 |
11 | BAA03g38660 | A03 | 17920010 | C | T | intron_variant | MODIFIER | c.498+182C>T| |
S33 |
12 | BAA03g38660 | A03 | 17920152 | C | T | intron_variant | MODIFIER | c.499-66C>T| |
S113 |
13 | BAA03g38660 | A03 | 17921987 | C | T | downstream_gene_variant | MODIFIER | c.*1239C>T| |
S53 |
14 | BAA03g38660 | A03 | 17922488 | G | A | downstream_gene_variant | MODIFIER | c.*1740G>A| |
S233 |
15 | BAA03g38660 | A03 | 17924230 | C | T | downstream_gene_variant | MODIFIER | c.*3482C>T| |
S67 |
16 | BAA03g38660 | A03 | 17924802 | C | T | downstream_gene_variant | MODIFIER | c.*4054C>T| |
S40 S49 |
17 | BAA03g38660 | A03 | 17925008 | G | A | downstream_gene_variant | MODIFIER | c.*4260G>A| |
S28 |