Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g31030 | A06 | 21125034 | G | A | upstream_gene_variant | MODIFIER | c.-3994G>A| |
S41 |
2 | BAA06g31030 | A06 | 21126022 | C | T | upstream_gene_variant | MODIFIER | c.-3006C>T| |
S293 |
3 | BAA06g31030 | A06 | 21126036 | C | T | upstream_gene_variant | MODIFIER | c.-2992C>T| |
S286 |
4 | BAA06g31030 | A06 | 21126115 | C | A | upstream_gene_variant | MODIFIER | c.-2913C>A| |
S212 |
5 | BAA06g31030 | A06 | 21126152 | T | A | upstream_gene_variant | MODIFIER | c.-2876T>A| |
S62 |
6 | BAA06g31030 | A06 | 21126634 | G | C | upstream_gene_variant | MODIFIER | c.-2394G>C| |
S299 |
7 | BAA06g31030 | A06 | 21126692 | C | T | upstream_gene_variant | MODIFIER | c.-2336C>T| |
S66 |
8 | BAA06g31030 | A06 | 21126815 | C | T | upstream_gene_variant | MODIFIER | c.-2213C>T| |
S113 S217 S248 |
9 | BAA06g31030 | A06 | 21127106 | C | T | upstream_gene_variant | MODIFIER | c.-1922C>T| |
S36 |
10 | BAA06g31030 | A06 | 21127300 | C | T | upstream_gene_variant | MODIFIER | c.-1728C>T| |
S298 |
11 | BAA06g31030 | A06 | 21127612 | G | A | upstream_gene_variant | MODIFIER | c.-1416G>A| |
S17 |
12 | BAA06g31030 | A06 | 21128055 | G | A | upstream_gene_variant | MODIFIER | c.-973G>A| |
S132 S137 S215 |
13 | BAA06g31030 | A06 | 21128198 | G | A | upstream_gene_variant | MODIFIER | c.-830G>A| |
S74 |
14 | BAA06g31030 | A06 | 21129262 | C | T | missense_variant | MODERATE | c.235C>T|p.Pro79Ser |
S80 |
15 | BAA06g31030 | A06 | 21129849 | G | A | missense_variant | MODERATE | c.655G>A|p.Asp219Asn |
S1 S90 |
16 | BAA06g31030 | A06 | 21129862 | G | A | missense_variant | MODERATE | c.668G>A|p.Gly223Glu |
S295 |
17 | BAA06g31030 | A06 | 21129918 | C | T | stop_gained | HIGH | c.724C>T|p.Gln242* |
S111 S301 S304 |
18 | BAA06g31030 | A06 | 21135097 | C | T | downstream_gene_variant | MODIFIER | c.*4639C>T| |
S280 |
19 | BAA06g31030 | A06 | 21135145 | G | A | downstream_gene_variant | MODIFIER | c.*4687G>A| |
S122 |