Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02110 | A10 | 987530 | C | T | upstream_gene_variant | MODIFIER | c.-3882C>T| |
S72 |
2 | BAA10g02110 | A10 | 988236 | G | A | upstream_gene_variant | MODIFIER | c.-3176G>A| |
S124 |
3 | BAA10g02110 | A10 | 988359 | G | A | upstream_gene_variant | MODIFIER | c.-3053G>A| |
S290 |
4 | BAA10g02110 | A10 | 989032 | G | A | upstream_gene_variant | MODIFIER | c.-2380G>A| |
S164 |
5 | BAA10g02110 | A10 | 989576 | C | T | upstream_gene_variant | MODIFIER | c.-1836C>T| |
S195 |
6 | BAA10g02110 | A10 | 991219 | G | A | upstream_gene_variant | MODIFIER | c.-193G>A| |
S296 |
7 | BAA10g02110 | A10 | 991411 | G | A | upstream_gene_variant | MODIFIER | c.-1G>A| |
S156 |
8 | BAA10g02110 | A10 | 991567 | C | T | synonymous_variant | LOW | c.156C>T|p.Ser52Ser |
S224 |
9 | BAA10g02110 | A10 | 992177 | G | A | missense_variant | MODERATE | c.412G>A|p.Val138Ile |
S62 |
10 | BAA10g02110 | A10 | 992641 | G | A | missense_variant | MODERATE | c.670G>A|p.Glu224Lys |
S292 |
11 | BAA10g02110 | A10 | 992664 | C | T | synonymous_variant | LOW | c.693C>T|p.Thr231Thr |
S11 |
12 | BAA10g02110 | A10 | 992802 | G | A | synonymous_variant | LOW | c.831G>A|p.Gln277Gln |
S242 |
13 | BAA10g02110 | A10 | 994225 | C | T | missense_variant | MODERATE | c.1937C>T|p.Pro646Leu |
S143 |
14 | BAA10g02110 | A10 | 994914 | G | A | synonymous_variant | LOW | c.2358G>A|p.Lys786Lys |
S215 |
15 | BAA10g02110 | A10 | 995387 | G | A | missense_variant | MODERATE | c.2725G>A|p.Glu909Lys |
S45 |
16 | BAA10g02110 | A10 | 995658 | C | T | downstream_gene_variant | MODIFIER | c.*116C>T| |
S165 |