Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g37850 | A07 | 34687514 | C | T | missense_variant | MODERATE | c.1804G>A|p.Asp602Asn |
S236 |
2 | BAA07g37850 | A07 | 34688416 | C | T | synonymous_variant | LOW | c.1329G>A|p.Gln443Gln |
S204 |
3 | BAA07g37850 | A07 | 34688470 | C | T | synonymous_variant | LOW | c.1275G>A|p.Glu425Glu |
S201 |
4 | BAA07g37850 | A07 | 34688612 | C | T | splice_donor_variant&intron_variant | HIGH | c.1212+1G>A| |
S42 |
5 | BAA07g37850 | A07 | 34689499 | C | T | missense_variant | MODERATE | c.754G>A|p.Gly252Arg |
S165 |
6 | BAA07g37850 | A07 | 34689738 | G | A | missense_variant | MODERATE | c.515C>T|p.Ser172Phe |
S79 S84 |
7 | BAA07g37850 | A07 | 34691523 | C | T | upstream_gene_variant | MODIFIER | c.-1063G>A| |
S167 |
8 | BAA07g37850 | A07 | 34692541 | C | T | upstream_gene_variant | MODIFIER | c.-2081G>A| |
S266 |
9 | BAA07g37850 | A07 | 34692760 | C | T | upstream_gene_variant | MODIFIER | c.-2300G>A| |
S286 |
10 | BAA07g37850 | A07 | 34692862 | C | T | upstream_gene_variant | MODIFIER | c.-2402G>A| |
S32 |
11 | BAA07g37850 | A07 | 34692972 | C | T | upstream_gene_variant | MODIFIER | c.-2512G>A| |
S173 |
12 | BAA07g37850 | A07 | 34695036 | C | T | upstream_gene_variant | MODIFIER | c.-4576G>A| |
S58 |