Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g10340 | A05 | 5249509 | C | T | upstream_gene_variant | MODIFIER | c.-4307C>T| |
S278 |
2 | BAA05g10340 | A05 | 5249677 | C | T | upstream_gene_variant | MODIFIER | c.-4139C>T| |
S67 |
3 | BAA05g10340 | A05 | 5250523 | G | A | upstream_gene_variant | MODIFIER | c.-3293G>A| |
S156 |
4 | BAA05g10340 | A05 | 5250575 | G | A | upstream_gene_variant | MODIFIER | c.-3241G>A| |
S15 S3 |
5 | BAA05g10340 | A05 | 5251374 | C | T | upstream_gene_variant | MODIFIER | c.-2442C>T| |
S305 |
6 | BAA05g10340 | A05 | 5251820 | C | T | upstream_gene_variant | MODIFIER | c.-1996C>T| |
S113 |
7 | BAA05g10340 | A05 | 5251834 | G | A | upstream_gene_variant | MODIFIER | c.-1982G>A| |
S186 |
8 | BAA05g10340 | A05 | 5253531 | C | T | upstream_gene_variant | MODIFIER | c.-285C>T| |
S251 |
9 | BAA05g10340 | A05 | 5254880 | C | T | splice_region_variant&intron_variant | LOW | c.673+7C>T| |
S278 |
10 | BAA05g10340 | A05 | 5255438 | C | T | missense_variant | MODERATE | c.1066C>T|p.His356Tyr |
S249 |
11 | BAA05g10340 | A05 | 5256587 | G | A | missense_variant | MODERATE | c.1909G>A|p.Asp637Asn |
S95 |
12 | BAA05g10340 | A05 | 5256700 | G | T | missense_variant | MODERATE | c.2022G>T|p.Gln674His |
S36 |