Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g03800 | A07 | 3114519 | C | T | upstream_gene_variant | MODIFIER | c.-4933C>T| |
S100 |
2 | BAA07g03800 | A07 | 3114746 | G | A | upstream_gene_variant | MODIFIER | c.-4706G>A| |
S108 |
3 | BAA07g03800 | A07 | 3116196 | C | T | upstream_gene_variant | MODIFIER | c.-3256C>T| |
S169 |
4 | BAA07g03800 | A07 | 3116526 | G | A | upstream_gene_variant | MODIFIER | c.-2926G>A| |
S223 |
5 | BAA07g03800 | A07 | 3116689 | C | T | upstream_gene_variant | MODIFIER | c.-2763C>T| |
S192 |
6 | BAA07g03800 | A07 | 3118193 | C | T | upstream_gene_variant | MODIFIER | c.-1259C>T| |
S19 S284 |
7 | BAA07g03800 | A07 | 3118238 | G | A | upstream_gene_variant | MODIFIER | c.-1214G>A| |
S296 |
8 | BAA07g03800 | A07 | 3118463 | G | A | upstream_gene_variant | MODIFIER | c.-989G>A| |
S296 |
9 | BAA07g03800 | A07 | 3118537 | C | T | upstream_gene_variant | MODIFIER | c.-915C>T| |
S169 |
10 | BAA07g03800 | A07 | 3121418 | G | A | missense_variant | MODERATE | c.827G>A|p.Gly276Glu |
S244 |
11 | BAA07g03800 | A07 | 3121801 | C | T | missense_variant | MODERATE | c.964C>T|p.Arg322Trp |
S152 |
12 | BAA07g03800 | A07 | 3121936 | C | T | synonymous_variant | LOW | c.1015C>T|p.Leu339Leu |
S252 |
13 | BAA07g03800 | A07 | 3123102 | G | A | missense_variant&splice_region_variant | MODERATE | c.1432G>A|p.Glu478Lys |
S176 |
14 | BAA07g03800 | A07 | 3126950 | C | T | downstream_gene_variant | MODIFIER | c.*3348C>T| |
S12 |
15 | BAA07g03800 | A07 | 3127024 | C | T | downstream_gene_variant | MODIFIER | c.*3422C>T| |
S212 |
16 | BAA07g03800 | A07 | 3127177 | G | A | downstream_gene_variant | MODIFIER | c.*3575G>A| |
S251 |
17 | BAA07g03800 | A07 | 3127978 | C | T | downstream_gene_variant | MODIFIER | c.*4376C>T| |
S232 |
18 | BAA07g03800 | A07 | 3128027 | T | C | downstream_gene_variant | MODIFIER | c.*4425T>C| |
S299 |