Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g35880 | A06 | 23892956 | C | T | missense_variant | MODERATE | c.2543G>A|p.Gly848Glu |
S235 S243 |
2 | BAA06g35880 | A06 | 23893113 | G | A | missense_variant | MODERATE | c.2386C>T|p.Leu796Phe |
S219 S72 |
3 | BAA06g35880 | A06 | 23893438 | G | A | synonymous_variant | LOW | c.2061C>T|p.Phe687Phe |
S28 |
4 | BAA06g35880 | A06 | 23894269 | G | A | missense_variant | MODERATE | c.1532C>T|p.Thr511Met |
S298 |
5 | BAA06g35880 | A06 | 23895326 | G | A | missense_variant | MODERATE | c.586C>T|p.Leu196Phe |
S225 |
6 | BAA06g35880 | A06 | 23895521 | G | A | synonymous_variant | LOW | c.391C>T|p.Leu131Leu |
S265 |
7 | BAA06g35880 | A06 | 23895820 | G | A | missense_variant | MODERATE | c.92C>T|p.Ala31Val |
S228 |
8 | BAA06g35880 | A06 | 23896022 | C | T | upstream_gene_variant | MODIFIER | c.-111G>A| |
S176 |
9 | BAA06g35880 | A06 | 23896132 | G | A | upstream_gene_variant | MODIFIER | c.-221C>T| |
S77 S82 |
10 | BAA06g35880 | A06 | 23896762 | C | T | upstream_gene_variant | MODIFIER | c.-851G>A| |
S279 |
11 | BAA06g35880 | A06 | 23897780 | C | T | upstream_gene_variant | MODIFIER | c.-1869G>A| |
S15 S3 |
12 | BAA06g35880 | A06 | 23897940 | G | A | upstream_gene_variant | MODIFIER | c.-2029C>T| |
S161 |
13 | BAA06g35880 | A06 | 23899160 | C | T | upstream_gene_variant | MODIFIER | c.-3249G>A| |
S52 |
14 | BAA06g35880 | A06 | 23899258 | C | T | upstream_gene_variant | MODIFIER | c.-3347G>A| |
S272 |
15 | BAA06g35880 | A06 | 23899279 | C | T | upstream_gene_variant | MODIFIER | c.-3368G>A| |
S296 |
16 | BAA06g35880 | A06 | 23899821 | C | T | upstream_gene_variant | MODIFIER | c.-3910G>A| |
S270 |