Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g26780 | A06 | 18401257 | G | A | downstream_gene_variant | MODIFIER | c.*4710C>T| |
S138 |
2 | BAA06g26780 | A06 | 18402209 | G | A | downstream_gene_variant | MODIFIER | c.*3758C>T| |
S201 |
3 | BAA06g26780 | A06 | 18402624 | G | A | downstream_gene_variant | MODIFIER | c.*3343C>T| |
S183 S198 |
4 | BAA06g26780 | A06 | 18402628 | C | T | downstream_gene_variant | MODIFIER | c.*3339G>A| |
S196 |
5 | BAA06g26780 | A06 | 18402787 | C | T | downstream_gene_variant | MODIFIER | c.*3180G>A| |
S252 |
6 | BAA06g26780 | A06 | 18406423 | C | T | synonymous_variant | LOW | c.1119G>A|p.Arg373Arg |
S79 S91 |
7 | BAA06g26780 | A06 | 18406913 | G | A | missense_variant | MODERATE | c.629C>T|p.Pro210Leu |
S67 |
8 | BAA06g26780 | A06 | 18407307 | G | A | missense_variant | MODERATE | c.235C>T|p.Pro79Ser |
S17 |
9 | BAA06g26780 | A06 | 18408204 | G | A | upstream_gene_variant | MODIFIER | c.-663C>T| |
S287 |
10 | BAA06g26780 | A06 | 18408466 | C | T | upstream_gene_variant | MODIFIER | c.-925G>A| |
S100 |
11 | BAA06g26780 | A06 | 18408577 | C | T | upstream_gene_variant | MODIFIER | c.-1036G>A| |
S43 |
12 | BAA06g26780 | A06 | 18408936 | C | T | upstream_gene_variant | MODIFIER | c.-1395G>A| |
S284 |
13 | BAA06g26780 | A06 | 18410090 | G | A | upstream_gene_variant | MODIFIER | c.-2549C>T| |
S123 |
14 | BAA06g26780 | A06 | 18410641 | G | A | upstream_gene_variant | MODIFIER | c.-3100C>T| |
S138 |
15 | BAA06g26780 | A06 | 18410661 | G | A | upstream_gene_variant | MODIFIER | c.-3120C>T| |
S302 |
16 | BAA06g26780 | A06 | 18411199 | C | T | upstream_gene_variant | MODIFIER | c.-3658G>A| |
S164 |
17 | BAA06g26780 | A06 | 18411232 | C | T | upstream_gene_variant | MODIFIER | c.-3691G>A| |
S18 |
18 | BAA06g26780 | A06 | 18411723 | G | A | upstream_gene_variant | MODIFIER | c.-4182C>T| |
S13 |
19 | BAA06g26780 | A06 | 18412197 | C | T | upstream_gene_variant | MODIFIER | c.-4656G>A| |
S236 |