Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07100 | A10 | 3954406 | C | T | upstream_gene_variant | MODIFIER | c.-4218C>T| |
S199 |
2 | BAA10g07100 | A10 | 3955085 | G | A | upstream_gene_variant | MODIFIER | c.-3539G>A| |
S133 |
3 | BAA10g07100 | A10 | 3955486 | G | A | upstream_gene_variant | MODIFIER | c.-3138G>A| |
S45 |
4 | BAA10g07100 | A10 | 3955563 | G | A | upstream_gene_variant | MODIFIER | c.-3061G>A| |
S263 |
5 | BAA10g07100 | A10 | 3955952 | C | T | upstream_gene_variant | MODIFIER | c.-2672C>T| |
S98 |
6 | BAA10g07100 | A10 | 3956076 | G | A | upstream_gene_variant | MODIFIER | c.-2548G>A| |
S128 |
7 | BAA10g07100 | A10 | 3957124 | G | A | upstream_gene_variant | MODIFIER | c.-1500G>A| |
S16 |
8 | BAA10g07100 | A10 | 3957471 | C | T | upstream_gene_variant | MODIFIER | c.-1153C>T| |
S11 |
9 | BAA10g07100 | A10 | 3957652 | G | A | upstream_gene_variant | MODIFIER | c.-972G>A| |
S187 |
10 | BAA10g07100 | A10 | 3958816 | G | A | missense_variant | MODERATE | c.193G>A|p.Asp65Asn |
S209 |
11 | BAA10g07100 | A10 | 3959372 | G | A | missense_variant | MODERATE | c.749G>A|p.Gly250Glu |
S82 S92 |
12 | BAA10g07100 | A10 | 3959383 | C | T | synonymous_variant | LOW | c.760C>T|p.Leu254Leu |
S294 |
13 | BAA10g07100 | A10 | 3960139 | G | A | missense_variant | MODERATE | c.1030G>A|p.Ala344Thr |
S33 |