Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g41290 | A07 | 36274165 | C | T | downstream_gene_variant | MODIFIER | c.*616G>A| |
S161 |
2 | BAA07g41290 | A07 | 36275726 | C | T | missense_variant | MODERATE | c.2461G>A|p.Glu821Lys |
S213 |
3 | BAA07g41290 | A07 | 36276053 | G | A | missense_variant | MODERATE | c.2134C>T|p.Pro712Ser |
S294 |
4 | BAA07g41290 | A07 | 36276626 | C | T | missense_variant&splice_region_variant | MODERATE | c.1646G>A|p.Arg549Lys |
S37 |
5 | BAA07g41290 | A07 | 36277051 | G | A | synonymous_variant | LOW | c.1380C>T|p.Ile460Ile |
S87 |
6 | BAA07g41290 | A07 | 36278053 | C | T | missense_variant | MODERATE | c.802G>A|p.Ala268Thr |
S282 |
7 | BAA07g41290 | A07 | 36279334 | G | A | missense_variant | MODERATE | c.152C>T|p.Ala51Val |
S76 |
8 | BAA07g41290 | A07 | 36279669 | C | T | upstream_gene_variant | MODIFIER | c.-184G>A| |
S266 |
9 | BAA07g41290 | A07 | 36281449 | G | A | upstream_gene_variant | MODIFIER | c.-1964C>T| |
S242 |
10 | BAA07g41290 | A07 | 36282149 | A | G | upstream_gene_variant | MODIFIER | c.-2664T>C| |
S201 |
11 | BAA07g41290 | A07 | 36282157 | C | T | upstream_gene_variant | MODIFIER | c.-2672G>A| |
S284 |
12 | BAA07g41290 | A07 | 36282399 | C | T | upstream_gene_variant | MODIFIER | c.-2914G>A| |
S286 |
13 | BAA07g41290 | A07 | 36283221 | G | A | upstream_gene_variant | MODIFIER | c.-3736C>T| |
S50 |
14 | BAA07g41290 | A07 | 36283481 | G | A | upstream_gene_variant | MODIFIER | c.-3996C>T| |
S163 |