Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g02500 | A05 | 1350640 | T | A | synonymous_variant | LOW | c.2484A>T|p.Ser828Ser |
S54 |
2 | BAA05g02500 | A05 | 1350738 | C | T | missense_variant | MODERATE | c.2386G>A|p.Ala796Thr |
S262 |
3 | BAA05g02500 | A05 | 1351507 | C | T | missense_variant | MODERATE | c.2158G>A|p.Asp720Asn |
S153 S213 |
4 | BAA05g02500 | A05 | 1352484 | C | T | synonymous_variant | LOW | c.1602G>A|p.Lys534Lys |
S268 |
5 | BAA05g02500 | A05 | 1353241 | G | A | splice_region_variant&intron_variant | LOW | c.1185+3C>T| |
S158 |
6 | BAA05g02500 | A05 | 1353710 | G | C | missense_variant | MODERATE | c.893C>G|p.Thr298Ser |
S265 |
7 | BAA05g02500 | A05 | 1354134 | C | T | missense_variant | MODERATE | c.703G>A|p.Ala235Thr |
S109 |
8 | BAA05g02500 | A05 | 1354264 | G | A | intron_variant | MODIFIER | c.641-68C>T| |
S23 |
9 | BAA05g02500 | A05 | 1354265 | G | A | intron_variant | MODIFIER | c.641-69C>T| |
S277 |
10 | BAA05g02500 | A05 | 1354560 | C | T | missense_variant | MODERATE | c.499G>A|p.Val167Met |
S87 |
11 | BAA05g02500 | A05 | 1355214 | G | A | missense_variant | MODERATE | c.110C>T|p.Ser37Phe |
S138 |
12 | BAA05g02500 | A05 | 1355614 | C | T | upstream_gene_variant | MODIFIER | c.-205G>A| |
S195 |
13 | BAA05g02500 | A05 | 1355826 | G | A | upstream_gene_variant | MODIFIER | c.-417C>T| |
S190 |
14 | BAA05g02500 | A05 | 1357076 | C | T | upstream_gene_variant | MODIFIER | c.-1667G>A| |
S162 |
15 | BAA05g02500 | A05 | 1357637 | G | A | upstream_gene_variant | MODIFIER | c.-2228C>T| |
S117 |
16 | BAA05g02500 | A05 | 1359018 | C | T | upstream_gene_variant | MODIFIER | c.-3609G>A| |
S197 |