Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08400 | A10 | 10141247 | C | T | missense_variant | MODERATE | c.1810G>A|p.Ala604Thr |
S155 S211 |
2 | BAA10g08400 | A10 | 10141378 | C | T | missense_variant | MODERATE | c.1679G>A|p.Arg560His |
S247 |
3 | BAA10g08400 | A10 | 10141741 | G | A | intron_variant | MODIFIER | c.1459-143C>T| |
S221 |
4 | BAA10g08400 | A10 | 10141797 | G | A | intron_variant | MODIFIER | c.1458+92C>T| |
S66 |
5 | BAA10g08400 | A10 | 10141969 | C | T | missense_variant | MODERATE | c.1378G>A|p.Asp460Asn |
S249 |
6 | BAA10g08400 | A10 | 10142339 | G | A | intron_variant | MODIFIER | c.1150-17C>T| |
S158 |
7 | BAA10g08400 | A10 | 10142526 | G | A | synonymous_variant | LOW | c.1035C>T|p.Asn345Asn |
S259 |
8 | BAA10g08400 | A10 | 10143135 | G | A | missense_variant | MODERATE | c.515C>T|p.Pro172Leu |
S38 |
9 | BAA10g08400 | A10 | 10143730 | G | A | upstream_gene_variant | MODIFIER | c.-17C>T| |
S18 |
10 | BAA10g08400 | A10 | 10145245 | G | A | upstream_gene_variant | MODIFIER | c.-1532C>T| |
S126 |
11 | BAA10g08400 | A10 | 10145882 | G | A | upstream_gene_variant | MODIFIER | c.-2169C>T| |
S148 S30 S31 |
12 | BAA10g08400 | A10 | 10147183 | G | A | upstream_gene_variant | MODIFIER | c.-3470C>T| |
S284 |
13 | BAA10g08400 | A10 | 10147652 | T | A | upstream_gene_variant | MODIFIER | c.-3939A>T| |
S205 |
14 | BAA10g08400 | A10 | 10148341 | C | T | upstream_gene_variant | MODIFIER | c.-4628G>A| |
S37 |