Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14010 | A10 | 14862795 | G | A | upstream_gene_variant | MODIFIER | c.-4157G>A| |
S157 S163 |
2 | BAA10g14010 | A10 | 14863136 | C | T | upstream_gene_variant | MODIFIER | c.-3816C>T| |
S161 |
3 | BAA10g14010 | A10 | 14863367 | G | A | upstream_gene_variant | MODIFIER | c.-3585G>A| |
S284 |
4 | BAA10g14010 | A10 | 14863417 | G | A | upstream_gene_variant | MODIFIER | c.-3535G>A| |
S139 |
5 | BAA10g14010 | A10 | 14863905 | C | T | upstream_gene_variant | MODIFIER | c.-3047C>T| |
S161 |
6 | BAA10g14010 | A10 | 14864697 | G | A | upstream_gene_variant | MODIFIER | c.-2255G>A| |
S292 |
7 | BAA10g14010 | A10 | 14866323 | C | T | upstream_gene_variant | MODIFIER | c.-629C>T| |
S281 |
8 | BAA10g14010 | A10 | 14868111 | C | T | intron_variant | MODIFIER | c.177+983C>T| |
S123 |
9 | BAA10g14010 | A10 | 14868362 | C | T | intron_variant | MODIFIER | c.177+1234C>T| |
S63 |
10 | BAA10g14010 | A10 | 14868365 | C | T | intron_variant | MODIFIER | c.177+1237C>T| |
S233 |
11 | BAA10g14010 | A10 | 14871971 | C | T | intron_variant | MODIFIER | c.178-1932C>T| |
S97 |
12 | BAA10g14010 | A10 | 14872223 | C | T | intron_variant | MODIFIER | c.178-1680C>T| |
S142 |
13 | BAA10g14010 | A10 | 14872235 | C | T | intron_variant | MODIFIER | c.178-1668C>T| |
S51 |
14 | BAA10g14010 | A10 | 14874094 | C | T | intron_variant | MODIFIER | c.296-48C>T| |
S270 |
15 | BAA10g14010 | A10 | 14874722 | G | A | intron_variant | MODIFIER | c.371-392G>A| |
S192 |
16 | BAA10g14010 | A10 | 14875390 | C | T | synonymous_variant | LOW | c.549C>T|p.Ser183Ser |
S161 |
17 | BAA10g14010 | A10 | 14875691 | C | T | missense_variant | MODERATE | c.850C>T|p.Arg284Cys |
S235 |
18 | BAA10g14010 | A10 | 14875772 | G | A | missense_variant | MODERATE | c.931G>A|p.Glu311Lys |
S55 |