Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g02130 | A07 | 1572892 | C | T | upstream_gene_variant | MODIFIER | c.-4611C>T| |
S1 S90 |
2 | BAA07g02130 | A07 | 1573467 | C | T | upstream_gene_variant | MODIFIER | c.-4036C>T| |
S156 |
3 | BAA07g02130 | A07 | 1573499 | C | T | upstream_gene_variant | MODIFIER | c.-4004C>T| |
S138 |
4 | BAA07g02130 | A07 | 1573993 | G | A | upstream_gene_variant | MODIFIER | c.-3510G>A| |
S225 S73 |
5 | BAA07g02130 | A07 | 1574634 | G | A | upstream_gene_variant | MODIFIER | c.-2869G>A| |
S235 S236 S260 |
6 | BAA07g02130 | A07 | 1574743 | C | T | upstream_gene_variant | MODIFIER | c.-2760C>T| |
S302 |
7 | BAA07g02130 | A07 | 1575089 | C | T | upstream_gene_variant | MODIFIER | c.-2414C>T| |
S155 S211 |
8 | BAA07g02130 | A07 | 1575995 | G | A | upstream_gene_variant | MODIFIER | c.-1508G>A| |
S275 |
9 | BAA07g02130 | A07 | 1576701 | C | T | upstream_gene_variant | MODIFIER | c.-802C>T| |
S148 |
10 | BAA07g02130 | A07 | 1577678 | C | T | missense_variant | MODERATE | c.176C>T|p.Ser59Leu |
S67 |
11 | BAA07g02130 | A07 | 1577805 | C | T | synonymous_variant | LOW | c.303C>T|p.Phe101Phe |
S161 |
12 | BAA07g02130 | A07 | 1577820 | C | T | synonymous_variant | LOW | c.318C>T|p.Ile106Ile |
S168 |
13 | BAA07g02130 | A07 | 1578049 | G | A | missense_variant | MODERATE | c.547G>A|p.Gly183Arg |
S56 |
14 | BAA07g02130 | A07 | 1579812 | C | T | downstream_gene_variant | MODIFIER | c.*1083C>T| |
S249 |
15 | BAA07g02130 | A07 | 1580115 | G | A | downstream_gene_variant | MODIFIER | c.*1386G>A| |
S105 S106 |
16 | BAA07g02130 | A07 | 1580253 | G | A | downstream_gene_variant | MODIFIER | c.*1524G>A| |
S46 |
17 | BAA07g02130 | A07 | 1580772 | G | A | downstream_gene_variant | MODIFIER | c.*2043G>A| |
S109 |
18 | BAA07g02130 | A07 | 1583045 | C | T | downstream_gene_variant | MODIFIER | c.*4316C>T| |
S152 |