Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g02580 | A01 | 1172415 | G | C | upstream_gene_variant | MODIFIER | c.-4531G>C| |
S266 |
2 | BAA01g02580 | A01 | 1175049 | C | T | upstream_gene_variant | MODIFIER | c.-1897C>T| |
S261 |
3 | BAA01g02580 | A01 | 1175616 | G | A | upstream_gene_variant | MODIFIER | c.-1330G>A| |
S264 |
4 | BAA01g02580 | A01 | 1176345 | G | A | upstream_gene_variant | MODIFIER | c.-601G>A| |
S297 |
5 | BAA01g02580 | A01 | 1176684 | G | A | upstream_gene_variant | MODIFIER | c.-262G>A| |
S60 |
6 | BAA01g02580 | A01 | 1176925 | C | T | upstream_gene_variant | MODIFIER | c.-21C>T| |
S107 |
7 | BAA01g02580 | A01 | 1177014 | C | T | synonymous_variant | LOW | c.69C>T|p.Val23Val |
S299 |
8 | BAA01g02580 | A01 | 1177115 | G | A | missense_variant | MODERATE | c.170G>A|p.Arg57Gln |
S204 |
9 | BAA01g02580 | A01 | 1179965 | C | T | missense_variant | MODERATE | c.1822C>T|p.Leu608Phe |
S267 |
10 | BAA01g02580 | A01 | 1180279 | C | T | splice_region_variant&intron_variant | LOW | c.2001-6C>T| |
S67 |
11 | BAA01g02580 | A01 | 1180307 | G | A | missense_variant | MODERATE | c.2023G>A|p.Glu675Lys |
S33 |
12 | BAA01g02580 | A01 | 1181234 | G | A | downstream_gene_variant | MODIFIER | c.*738G>A| |
S37 |
13 | BAA01g02580 | A01 | 1181920 | G | A | downstream_gene_variant | MODIFIER | c.*1424G>A| |
S157 S163 |
14 | BAA01g02580 | A01 | 1183558 | C | T | downstream_gene_variant | MODIFIER | c.*3062C>T| |
S46 |
15 | BAA01g02580 | A01 | 1184622 | C | T | downstream_gene_variant | MODIFIER | c.*4126C>T| |
S90 |
16 | BAA01g02580 | A01 | 1184800 | C | T | downstream_gene_variant | MODIFIER | c.*4304C>T| |
S19 |
17 | BAA01g02580 | A01 | 1184819 | G | A | downstream_gene_variant | MODIFIER | c.*4323G>A| |
S140 |
18 | BAA01g02580 | A01 | 1184972 | G | A | downstream_gene_variant | MODIFIER | c.*4476G>A| |
S191 |