Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49740 | A09 | 52947468 | C | T | missense_variant | MODERATE | c.3835G>A|p.Glu1279Lys |
S5 |
2 | BAA09g49740 | A09 | 52947504 | C | T | missense_variant | MODERATE | c.3799G>A|p.Gly1267Arg |
S229 |
3 | BAA09g49740 | A09 | 52947895 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.3550-1G>A| |
S173 |
4 | BAA09g49740 | A09 | 52949639 | G | A | synonymous_variant | LOW | c.2562C>T|p.Ser854Ser |
S276 |
5 | BAA09g49740 | A09 | 52949977 | C | T | missense_variant | MODERATE | c.2224G>A|p.Asp742Asn |
S260 |
6 | BAA09g49740 | A09 | 52951290 | C | T | missense_variant | MODERATE | c.1195G>A|p.Glu399Lys |
S260 |
7 | BAA09g49740 | A09 | 52951464 | C | T | missense_variant | MODERATE | c.1021G>A|p.Ala341Thr |
S67 |
8 | BAA09g49740 | A09 | 52952896 | G | A | upstream_gene_variant | MODIFIER | c.-26C>T| |
S136 |
9 | BAA09g49740 | A09 | 52953675 | G | A | upstream_gene_variant | MODIFIER | c.-805C>T| |
S151 S263 |
10 | BAA09g49740 | A09 | 52954234 | C | T | upstream_gene_variant | MODIFIER | c.-1364G>A| |
S226 |
11 | BAA09g49740 | A09 | 52956651 | G | A | upstream_gene_variant | MODIFIER | c.-3781C>T| |
S2 |
12 | BAA09g49740 | A09 | 52957275 | C | T | upstream_gene_variant | MODIFIER | c.-4405G>A| |
S138 |