Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g00950 | A06 | 647065 | G | A | upstream_gene_variant | MODIFIER | c.-4078G>A| |
S186 |
2 | BAA06g00950 | A06 | 647859 | C | T | upstream_gene_variant | MODIFIER | c.-3284C>T| |
S92 |
3 | BAA06g00950 | A06 | 648454 | G | A | upstream_gene_variant | MODIFIER | c.-2689G>A| |
S191 |
4 | BAA06g00950 | A06 | 649514 | G | A | upstream_gene_variant | MODIFIER | c.-1629G>A| |
S244 |
5 | BAA06g00950 | A06 | 650086 | G | A | upstream_gene_variant | MODIFIER | c.-1057G>A| |
S71 |
6 | BAA06g00950 | A06 | 650378 | G | A | upstream_gene_variant | MODIFIER | c.-765G>A| |
S42 |
7 | BAA06g00950 | A06 | 650393 | C | T | upstream_gene_variant | MODIFIER | c.-750C>T| |
S305 |
8 | BAA06g00950 | A06 | 651073 | C | T | upstream_gene_variant | MODIFIER | c.-70C>T| |
S228 |
9 | BAA06g00950 | A06 | 651946 | G | A | missense_variant | MODERATE | c.566G>A|p.Gly189Glu |
S190 |
10 | BAA06g00950 | A06 | 651969 | G | A | missense_variant | MODERATE | c.589G>A|p.Gly197Arg |
S112 |
11 | BAA06g00950 | A06 | 652264 | G | A | missense_variant | MODERATE | c.884G>A|p.Gly295Glu |
S201 |
12 | BAA06g00950 | A06 | 652351 | G | A | missense_variant | MODERATE | c.971G>A|p.Gly324Glu |
S267 |