Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g04000 | A08 | 2784727 | C | T | upstream_gene_variant | MODIFIER | c.-1742C>T| |
S67 |
2 | BAA08g04000 | A08 | 2784770 | C | T | upstream_gene_variant | MODIFIER | c.-1699C>T| |
S7 |
3 | BAA08g04000 | A08 | 2785356 | C | T | upstream_gene_variant | MODIFIER | c.-1113C>T| |
S280 |
4 | BAA08g04000 | A08 | 2785493 | C | T | upstream_gene_variant | MODIFIER | c.-976C>T| |
S149 |
5 | BAA08g04000 | A08 | 2786340 | C | T | upstream_gene_variant | MODIFIER | c.-129C>T| |
S243 S299 |
6 | BAA08g04000 | A08 | 2786513 | G | A | synonymous_variant | LOW | c.45G>A|p.Glu15Glu |
S236 |
7 | BAA08g04000 | A08 | 2786901 | G | A | missense_variant | MODERATE | c.364G>A|p.Asp122Asn |
S148 |
8 | BAA08g04000 | A08 | 2787215 | C | T | intron_variant | MODIFIER | c.400-140C>T| |
S152 |
9 | BAA08g04000 | A08 | 2787412 | C | T | synonymous_variant | LOW | c.457C>T|p.Leu153Leu |
S175 |
10 | BAA08g04000 | A08 | 2787574 | G | A | missense_variant | MODERATE | c.529G>A|p.Val177Ile |
S217 S248 |
11 | BAA08g04000 | A08 | 2789001 | C | T | intron_variant | MODIFIER | c.752-840C>T| |
S46 |
12 | BAA08g04000 | A08 | 2789084 | C | T | intron_variant | MODIFIER | c.752-757C>T| |
S170 |