Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44380 | A01 | 29488640 | G | A | downstream_gene_variant | MODIFIER | c.*2752C>T| |
S284 |
2 | BAA01g44380 | A01 | 29489868 | C | T | downstream_gene_variant | MODIFIER | c.*1524G>A| |
S12 |
3 | BAA01g44380 | A01 | 29491179 | C | T | downstream_gene_variant | MODIFIER | c.*213G>A| |
S18 |
4 | BAA01g44380 | A01 | 29491212 | G | A | downstream_gene_variant | MODIFIER | c.*180C>T| |
S114 |
5 | BAA01g44380 | A01 | 29491407 | C | G | missense_variant | MODERATE | c.801G>C|p.Met267Ile |
S115 |
6 | BAA01g44380 | A01 | 29491459 | G | A | missense_variant | MODERATE | c.749C>T|p.Ala250Val |
S139 |
7 | BAA01g44380 | A01 | 29491464 | G | A | synonymous_variant | LOW | c.744C>T|p.Leu248Leu |
S10 |
8 | BAA01g44380 | A01 | 29491507 | C | T | missense_variant | MODERATE | c.701G>A|p.Gly234Glu |
S256 |
9 | BAA01g44380 | A01 | 29492972 | C | T | upstream_gene_variant | MODIFIER | c.-765G>A| |
S210 S225 |
10 | BAA01g44380 | A01 | 29493568 | C | T | upstream_gene_variant | MODIFIER | c.-1361G>A| |
S94 |
11 | BAA01g44380 | A01 | 29493971 | G | A | upstream_gene_variant | MODIFIER | c.-1764C>T| |
S250 |
12 | BAA01g44380 | A01 | 29494580 | C | T | upstream_gene_variant | MODIFIER | c.-2373G>A| |
S25 |
13 | BAA01g44380 | A01 | 29495174 | C | T | upstream_gene_variant | MODIFIER | c.-2967G>A| |
S47 |
14 | BAA01g44380 | A01 | 29495386 | G | A | upstream_gene_variant | MODIFIER | c.-3179C>T| |
S151 S153 S157 S167 S236 S262 S263 |
15 | BAA01g44380 | A01 | 29495935 | C | T | upstream_gene_variant | MODIFIER | c.-3728G>A| |
S42 |
16 | BAA01g44380 | A01 | 29496888 | C | T | upstream_gene_variant | MODIFIER | c.-4681G>A| |
S276 |
17 | BAA01g44380 | A01 | 29497021 | C | T | upstream_gene_variant | MODIFIER | c.-4814G>A| |
S171 |