Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g23560 | A09 | 14950440 | G | A | synonymous_variant | LOW | c.1590C>T|p.Tyr530Tyr |
S70 |
2 | BAA09g23560 | A09 | 14950551 | G | A | synonymous_variant | LOW | c.1479C>T|p.Ile493Ile |
S13 |
3 | BAA09g23560 | A09 | 14950645 | T | G | missense_variant | MODERATE | c.1385A>C|p.Glu462Ala |
S88 |
4 | BAA09g23560 | A09 | 14950685 | C | T | missense_variant | MODERATE | c.1345G>A|p.Ala449Thr |
S111 |
5 | BAA09g23560 | A09 | 14952137 | C | T | missense_variant | MODERATE | c.1013G>A|p.Gly338Glu |
S59 |
6 | BAA09g23560 | A09 | 14952303 | C | T | missense_variant | MODERATE | c.847G>A|p.Asp283Asn |
S242 |
7 | BAA09g23560 | A09 | 14952468 | G | A | missense_variant | MODERATE | c.682C>T|p.Pro228Ser |
S175 S244 |
8 | BAA09g23560 | A09 | 14952686 | G | A | intron_variant | MODIFIER | c.543-79C>T| |
S166 |
9 | BAA09g23560 | A09 | 14953151 | G | A | intron_variant | MODIFIER | c.465-31C>T| |
S246 |
10 | BAA09g23560 | A09 | 14954839 | G | A | synonymous_variant | LOW | c.120C>T|p.Leu40Leu |
S295 |
11 | BAA09g23560 | A09 | 14955283 | G | A | upstream_gene_variant | MODIFIER | c.-325C>T| |
S251 |
12 | BAA09g23560 | A09 | 14956014 | G | A | upstream_gene_variant | MODIFIER | c.-1056C>T| |
S89 |
13 | BAA09g23560 | A09 | 14957199 | C | T | upstream_gene_variant | MODIFIER | c.-2241G>A| |
S295 |
14 | BAA09g23560 | A09 | 14958703 | C | T | upstream_gene_variant | MODIFIER | c.-3745G>A| |
S148 |
15 | BAA09g23560 | A09 | 14959162 | C | T | upstream_gene_variant | MODIFIER | c.-4204G>A| |
S179 |
16 | BAA09g23560 | A09 | 14959294 | C | T | upstream_gene_variant | MODIFIER | c.-4336G>A| |
S277 |
17 | BAA09g23560 | A09 | 14959589 | G | A | upstream_gene_variant | MODIFIER | c.-4631C>T| |
S262 |