Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01450 | A08 | 1066936 | C | T | upstream_gene_variant | MODIFIER | c.-3122C>T| |
S183 S198 |
2 | BAA08g01450 | A08 | 1067103 | G | A | upstream_gene_variant | MODIFIER | c.-2955G>A| |
S224 |
3 | BAA08g01450 | A08 | 1067116 | C | T | upstream_gene_variant | MODIFIER | c.-2942C>T| |
S143 |
4 | BAA08g01450 | A08 | 1067145 | C | T | upstream_gene_variant | MODIFIER | c.-2913C>T| |
S148 S30 S31 |
5 | BAA08g01450 | A08 | 1068600 | G | A | upstream_gene_variant | MODIFIER | c.-1458G>A| |
S200 |
6 | BAA08g01450 | A08 | 1069326 | G | A | upstream_gene_variant | MODIFIER | c.-732G>A| |
S122 |
7 | BAA08g01450 | A08 | 1069676 | G | A | upstream_gene_variant | MODIFIER | c.-382G>A| |
S188 |
8 | BAA08g01450 | A08 | 1070940 | G | A | missense_variant | MODERATE | c.517G>A|p.Val173Met |
S229 |
9 | BAA08g01450 | A08 | 1071051 | G | A | intron_variant | MODIFIER | c.609+19G>A| |
S266 |
10 | BAA08g01450 | A08 | 1073012 | C | T | downstream_gene_variant | MODIFIER | c.*1072C>T| |
S275 |
11 | BAA08g01450 | A08 | 1073274 | G | A | downstream_gene_variant | MODIFIER | c.*1334G>A| |
S116 |
12 | BAA08g01450 | A08 | 1074151 | G | A | downstream_gene_variant | MODIFIER | c.*2211G>A| |
S279 |
13 | BAA08g01450 | A08 | 1074278 | C | T | downstream_gene_variant | MODIFIER | c.*2338C>T| |
S81 S85 |
14 | BAA08g01450 | A08 | 1074816 | C | T | downstream_gene_variant | MODIFIER | c.*2876C>T| |
S134 S183 |
15 | BAA08g01450 | A08 | 1075323 | G | A | downstream_gene_variant | MODIFIER | c.*3383G>A| |
S246 |
16 | BAA08g01450 | A08 | 1076367 | G | A | downstream_gene_variant | MODIFIER | c.*4427G>A| |
S279 |