Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g13360 | A07 | 21354672 | G | A | upstream_gene_variant | MODIFIER | c.-4776G>A| |
S251 |
2 | BAA07g13360 | A07 | 21355534 | G | A | upstream_gene_variant | MODIFIER | c.-3914G>A| |
S115 |
3 | BAA07g13360 | A07 | 21356014 | G | A | upstream_gene_variant | MODIFIER | c.-3434G>A| |
S46 |
4 | BAA07g13360 | A07 | 21356195 | C | T | upstream_gene_variant | MODIFIER | c.-3253C>T| |
S42 |
5 | BAA07g13360 | A07 | 21356973 | C | T | upstream_gene_variant | MODIFIER | c.-2475C>T| |
S200 |
6 | BAA07g13360 | A07 | 21357522 | C | T | upstream_gene_variant | MODIFIER | c.-1926C>T| |
S148 S210 |
7 | BAA07g13360 | A07 | 21358867 | C | T | upstream_gene_variant | MODIFIER | c.-581C>T| |
S260 |
8 | BAA07g13360 | A07 | 21359046 | C | T | upstream_gene_variant | MODIFIER | c.-402C>T| |
S169 S68 |
9 | BAA07g13360 | A07 | 21359155 | C | T | upstream_gene_variant | MODIFIER | c.-293C>T| |
S107 |
10 | BAA07g13360 | A07 | 21359570 | G | A | synonymous_variant | LOW | c.123G>A|p.Leu41Leu |
S48 |
11 | BAA07g13360 | A07 | 21359667 | C | T | synonymous_variant | LOW | c.220C>T|p.Leu74Leu |
S249 |
12 | BAA07g13360 | A07 | 21359838 | G | A | missense_variant | MODERATE | c.391G>A|p.Ala131Thr |
S54 |
13 | BAA07g13360 | A07 | 21360031 | C | T | missense_variant | MODERATE | c.584C>T|p.Ser195Phe |
S245 |
14 | BAA07g13360 | A07 | 21360089 | C | T | synonymous_variant | LOW | c.642C>T|p.Leu214Leu |
S121 |
15 | BAA07g13360 | A07 | 21360332 | C | T | synonymous_variant | LOW | c.885C>T|p.Ile295Ile |
S58 |
16 | BAA07g13360 | A07 | 21360397 | G | A | missense_variant | MODERATE | c.950G>A|p.Gly317Glu |
S6 |
17 | BAA07g13360 | A07 | 21362118 | C | T | downstream_gene_variant | MODIFIER | c.*1573C>T| |
S8 |
18 | BAA07g13360 | A07 | 21362476 | G | A | downstream_gene_variant | MODIFIER | c.*1931G>A| |
S172 S217 |
19 | BAA07g13360 | A07 | 21363440 | G | A | downstream_gene_variant | MODIFIER | c.*2895G>A| |
S268 |