Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05450 | A08 | 4150881 | C | T | downstream_gene_variant | MODIFIER | c.*1424G>A| |
S134 |
2 | BAA08g05450 | A08 | 4151177 | C | T | downstream_gene_variant | MODIFIER | c.*1128G>A| |
S73 |
3 | BAA08g05450 | A08 | 4151620 | C | T | downstream_gene_variant | MODIFIER | c.*685G>A| |
S144 |
4 | BAA08g05450 | A08 | 4152008 | G | A | downstream_gene_variant | MODIFIER | c.*297C>T| |
S58 |
5 | BAA08g05450 | A08 | 4152520 | C | T | missense_variant | MODERATE | c.721G>A|p.Glu241Lys |
S168 |
6 | BAA08g05450 | A08 | 4153209 | G | A | missense_variant | MODERATE | c.350C>T|p.Ala117Val |
S267 |
7 | BAA08g05450 | A08 | 4153221 | G | A | missense_variant | MODERATE | c.338C>T|p.Ser113Phe |
S263 |
8 | BAA08g05450 | A08 | 4153409 | G | A | splice_region_variant&synonymous_variant | LOW | c.150C>T|p.Phe50Phe |
S38 |
9 | BAA08g05450 | A08 | 4153425 | G | A | intron_variant | MODIFIER | c.149-15C>T| |
S192 |
10 | BAA08g05450 | A08 | 4154775 | C | T | upstream_gene_variant | MODIFIER | c.-1038G>A| |
S86 |
11 | BAA08g05450 | A08 | 4154840 | G | A | upstream_gene_variant | MODIFIER | c.-1103C>T| |
S139 |
12 | BAA08g05450 | A08 | 4156810 | C | T | upstream_gene_variant | MODIFIER | c.-3073G>A| |
S47 |
13 | BAA08g05450 | A08 | 4157009 | G | A | upstream_gene_variant | MODIFIER | c.-3272C>T| |
S187 |
14 | BAA08g05450 | A08 | 4157388 | G | A | upstream_gene_variant | MODIFIER | c.-3651C>T| |
S237 |
15 | BAA08g05450 | A08 | 4158234 | G | A | upstream_gene_variant | MODIFIER | c.-4497C>T| |
S81 S85 |
16 | BAA08g05450 | A08 | 4158607 | G | A | upstream_gene_variant | MODIFIER | c.-4870C>T| |
S202 |
17 | BAA08g05450 | A08 | 4158700 | G | A | upstream_gene_variant | MODIFIER | c.-4963C>T| |
S34 |