Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g28830 | A10 | 21945488 | C | T | upstream_gene_variant | MODIFIER | c.-4593C>T| |
S295 |
2 | BAA10g28830 | A10 | 21945618 | C | T | upstream_gene_variant | MODIFIER | c.-4463C>T| |
S119 |
3 | BAA10g28830 | A10 | 21946228 | C | T | upstream_gene_variant | MODIFIER | c.-3853C>T| |
S10 |
4 | BAA10g28830 | A10 | 21946495 | G | A | upstream_gene_variant | MODIFIER | c.-3586G>A| |
S217 |
5 | BAA10g28830 | A10 | 21946998 | C | T | upstream_gene_variant | MODIFIER | c.-3083C>T| |
S51 |
6 | BAA10g28830 | A10 | 21948170 | G | A | upstream_gene_variant | MODIFIER | c.-1911G>A| |
S18 |
7 | BAA10g28830 | A10 | 21948907 | C | T | upstream_gene_variant | MODIFIER | c.-1174C>T| |
S247 |
8 | BAA10g28830 | A10 | 21949627 | C | T | upstream_gene_variant | MODIFIER | c.-454C>T| |
S54 |
9 | BAA10g28830 | A10 | 21950696 | G | A | missense_variant | MODERATE | c.616G>A|p.Val206Ile |
S271 |
10 | BAA10g28830 | A10 | 21950839 | G | A | synonymous_variant | LOW | c.759G>A|p.Gln253Gln |
S115 |
11 | BAA10g28830 | A10 | 21951023 | G | A | missense_variant | MODERATE | c.943G>A|p.Gly315Arg |
S194 |
12 | BAA10g28830 | A10 | 21951071 | G | A | missense_variant | MODERATE | c.991G>A|p.Val331Ile |
S239 |
13 | BAA10g28830 | A10 | 21951254 | C | T | stop_gained | HIGH | c.1174C>T|p.Gln392* |
S8 |
14 | BAA10g28830 | A10 | 21951331 | G | A | synonymous_variant | LOW | c.1251G>A|p.Gln417Gln |
S176 |
15 | BAA10g28830 | A10 | 21951377 | G | A | missense_variant | MODERATE | c.1297G>A|p.Val433Met |
S71 |