Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g37530 | A09 | 45655999 | G | A | upstream_gene_variant | MODIFIER | c.-3376G>A| |
S167 |
2 | BAA09g37530 | A09 | 45656363 | G | A | upstream_gene_variant | MODIFIER | c.-3012G>A| |
S276 |
3 | BAA09g37530 | A09 | 45656520 | G | A | upstream_gene_variant | MODIFIER | c.-2855G>A| |
S132 S137 S215 S89 |
4 | BAA09g37530 | A09 | 45657123 | G | A | upstream_gene_variant | MODIFIER | c.-2252G>A| |
S262 |
5 | BAA09g37530 | A09 | 45657221 | G | A | upstream_gene_variant | MODIFIER | c.-2154G>A| |
S261 |
6 | BAA09g37530 | A09 | 45657690 | C | T | upstream_gene_variant | MODIFIER | c.-1685C>T| |
S142 |
7 | BAA09g37530 | A09 | 45657812 | C | T | upstream_gene_variant | MODIFIER | c.-1563C>T| |
S272 |
8 | BAA09g37530 | A09 | 45658110 | G | A | upstream_gene_variant | MODIFIER | c.-1265G>A| |
S148 S210 |
9 | BAA09g37530 | A09 | 45658352 | G | A | upstream_gene_variant | MODIFIER | c.-1023G>A| |
S202 |
10 | BAA09g37530 | A09 | 45658680 | G | A | upstream_gene_variant | MODIFIER | c.-695G>A| |
S67 |
11 | BAA09g37530 | A09 | 45659186 | C | T | upstream_gene_variant | MODIFIER | c.-189C>T| |
S186 |
12 | BAA09g37530 | A09 | 45659222 | G | A | upstream_gene_variant | MODIFIER | c.-153G>A| |
S62 |
13 | BAA09g37530 | A09 | 45659429 | C | T | missense_variant | MODERATE | c.55C>T|p.Leu19Phe |
S187 |
14 | BAA09g37530 | A09 | 45659657 | G | A | splice_region_variant&intron_variant | LOW | c.114-8G>A| |
S209 |
15 | BAA09g37530 | A09 | 45662315 | G | A | missense_variant | MODERATE | c.1223G>A|p.Gly408Glu |
S81 S85 |
16 | BAA09g37530 | A09 | 45662588 | C | T | missense_variant | MODERATE | c.1496C>T|p.Ser499Phe |
S241 |
17 | BAA09g37530 | A09 | 45662630 | G | A | missense_variant | MODERATE | c.1538G>A|p.Gly513Glu |
S132 S137 S215 S89 |
18 | BAA09g37530 | A09 | 45662862 | C | T | missense_variant | MODERATE | c.1682C>T|p.Ala561Val |
S279 |
19 | BAA09g37530 | A09 | 45663377 | G | A | synonymous_variant | LOW | c.1953G>A|p.Ala651Ala |
S292 |