Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g13300 | A08 | 11535655 | G | A | upstream_gene_variant | MODIFIER | c.-4992G>A| |
S11 |
2 | BAA08g13300 | A08 | 11536005 | G | A | upstream_gene_variant | MODIFIER | c.-4642G>A| |
S116 |
3 | BAA08g13300 | A08 | 11536107 | G | A | upstream_gene_variant | MODIFIER | c.-4540G>A| |
S121 |
4 | BAA08g13300 | A08 | 11536498 | G | A | upstream_gene_variant | MODIFIER | c.-4149G>A| |
S153 |
5 | BAA08g13300 | A08 | 11538717 | G | A | upstream_gene_variant | MODIFIER | c.-1930G>A| |
S115 |
6 | BAA08g13300 | A08 | 11539231 | C | T | upstream_gene_variant | MODIFIER | c.-1416C>T| |
S59 |
7 | BAA08g13300 | A08 | 11539613 | C | T | upstream_gene_variant | MODIFIER | c.-1034C>T| |
S202 |
8 | BAA08g13300 | A08 | 11540596 | C | T | upstream_gene_variant | MODIFIER | c.-51C>T| |
S240 |
9 | BAA08g13300 | A08 | 11540816 | C | T | missense_variant | MODERATE | c.170C>T|p.Ala57Val |
S162 |
10 | BAA08g13300 | A08 | 11541273 | C | T | missense_variant | MODERATE | c.461C>T|p.Thr154Ile |
S126 |
11 | BAA08g13300 | A08 | 11543884 | C | T | intron_variant | MODIFIER | c.1403-43C>T| |
S169 |
12 | BAA08g13300 | A08 | 11544256 | G | A | missense_variant | MODERATE | c.1573G>A|p.Ala525Thr |
S188 |
13 | BAA08g13300 | A08 | 11544426 | G | A | intron_variant | MODIFIER | c.1645-12G>A| |
S232 |
14 | BAA08g13300 | A08 | 11545049 | C | T | missense_variant | MODERATE | c.2017C>T|p.Pro673Ser |
S139 |
15 | BAA08g13300 | A08 | 11545663 | G | A | missense_variant | MODERATE | c.2290G>A|p.Asp764Asn |
S232 |
16 | BAA08g13300 | A08 | 11550999 | G | A | downstream_gene_variant | MODIFIER | c.*4241G>A| |
S65 |