Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g12650 | A07 | 20874413 | G | A | splice_region_variant&intron_variant | LOW | c.3028-3C>T| |
S259 |
2 | BAA07g12650 | A07 | 20874674 | G | A | splice_region_variant&intron_variant | LOW | c.2946+8C>T| |
S259 |
3 | BAA07g12650 | A07 | 20875448 | G | T | synonymous_variant | LOW | c.2608C>A|p.Arg870Arg |
S245 |
4 | BAA07g12650 | A07 | 20876018 | C | T | synonymous_variant | LOW | c.2283G>A|p.Glu761Glu |
S75 S81 |
5 | BAA07g12650 | A07 | 20876515 | C | T | missense_variant | MODERATE | c.2126G>A|p.Gly709Glu |
S47 |
6 | BAA07g12650 | A07 | 20877211 | C | T | missense_variant&splice_region_variant | MODERATE | c.1849G>A|p.Glu617Lys |
S35 |
7 | BAA07g12650 | A07 | 20878683 | C | T | missense_variant | MODERATE | c.1160G>A|p.Arg387His |
S204 |
8 | BAA07g12650 | A07 | 20879698 | G | A | missense_variant | MODERATE | c.805C>T|p.Pro269Ser |
S109 |
9 | BAA07g12650 | A07 | 20880106 | C | T | synonymous_variant | LOW | c.576G>A|p.Lys192Lys |
S277 |
10 | BAA07g12650 | A07 | 20880496 | G | A | synonymous_variant | LOW | c.405C>T|p.Pro135Pro |
S226 |
11 | BAA07g12650 | A07 | 20881360 | G | A | upstream_gene_variant | MODIFIER | c.-207C>T| |
S62 |
12 | BAA07g12650 | A07 | 20881534 | G | A | upstream_gene_variant | MODIFIER | c.-381C>T| |
S48 |
13 | BAA07g12650 | A07 | 20882898 | G | A | upstream_gene_variant | MODIFIER | c.-1745C>T| |
S272 |
14 | BAA07g12650 | A07 | 20883168 | C | T | upstream_gene_variant | MODIFIER | c.-2015G>A| |
S36 |
15 | BAA07g12650 | A07 | 20884770 | C | T | upstream_gene_variant | MODIFIER | c.-3617G>A| |
S4 |
16 | BAA07g12650 | A07 | 20884869 | C | T | upstream_gene_variant | MODIFIER | c.-3716G>A| |
S213 |
17 | BAA07g12650 | A07 | 20885142 | G | A | upstream_gene_variant | MODIFIER | c.-3989C>T| |
S183 |