Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g41170 | A06 | 26797086 | C | T | missense_variant&splice_region_variant | MODERATE | c.2536G>A|p.Glu846Lys |
S282 |
2 | BAA06g41170 | A06 | 26798443 | C | T | missense_variant | MODERATE | c.1609G>A|p.Glu537Lys |
S257 |
3 | BAA06g41170 | A06 | 26798892 | G | A | missense_variant | MODERATE | c.1160C>T|p.Pro387Leu |
S273 |
4 | BAA06g41170 | A06 | 26799059 | C | T | synonymous_variant | LOW | c.993G>A|p.Gln331Gln |
S116 |
5 | BAA06g41170 | A06 | 26800570 | C | T | upstream_gene_variant | MODIFIER | c.-329G>A| |
S244 S266 |
6 | BAA06g41170 | A06 | 26800932 | G | A | upstream_gene_variant | MODIFIER | c.-691C>T| |
S283 |
7 | BAA06g41170 | A06 | 26801980 | C | T | upstream_gene_variant | MODIFIER | c.-1739G>A| |
S111 |
8 | BAA06g41170 | A06 | 26802486 | C | T | upstream_gene_variant | MODIFIER | c.-2245G>A| |
S124 |
9 | BAA06g41170 | A06 | 26802637 | C | T | upstream_gene_variant | MODIFIER | c.-2396G>A| |
S46 |
10 | BAA06g41170 | A06 | 26803440 | C | T | upstream_gene_variant | MODIFIER | c.-3199G>A| |
S252 |
11 | BAA06g41170 | A06 | 26803916 | C | T | upstream_gene_variant | MODIFIER | c.-3675G>A| |
S294 |