Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09290 | A10 | 11285131 | C | T | missense_variant | MODERATE | c.725G>A|p.Ser242Asn |
S28 |
2 | BAA10g09290 | A10 | 11285680 | G | A | missense_variant | MODERATE | c.323C>T|p.Ser108Phe |
S65 |
3 | BAA10g09290 | A10 | 11285779 | G | A | missense_variant | MODERATE | c.224C>T|p.Ala75Val |
S274 |
4 | BAA10g09290 | A10 | 11285944 | G | A | missense_variant | MODERATE | c.59C>T|p.Ala20Val |
S226 |
5 | BAA10g09290 | A10 | 11285950 | G | A | missense_variant | MODERATE | c.53C>T|p.Ser18Phe |
S192 S291 |
6 | BAA10g09290 | A10 | 11286102 | G | A | upstream_gene_variant | MODIFIER | c.-100C>T| |
S107 |
7 | BAA10g09290 | A10 | 11286154 | G | A | upstream_gene_variant | MODIFIER | c.-152C>T| |
S209 |
8 | BAA10g09290 | A10 | 11286283 | G | A | upstream_gene_variant | MODIFIER | c.-281C>T| |
S308 |
9 | BAA10g09290 | A10 | 11286668 | G | A | upstream_gene_variant | MODIFIER | c.-666C>T| |
S32 |
10 | BAA10g09290 | A10 | 11287033 | G | A | upstream_gene_variant | MODIFIER | c.-1031C>T| |
S66 |
11 | BAA10g09290 | A10 | 11287498 | G | A | upstream_gene_variant | MODIFIER | c.-1496C>T| |
S289 |
12 | BAA10g09290 | A10 | 11287960 | G | A | upstream_gene_variant | MODIFIER | c.-1958C>T| |
S273 |
13 | BAA10g09290 | A10 | 11288860 | T | C | upstream_gene_variant | MODIFIER | c.-2858A>G| |
S192 |
14 | BAA10g09290 | A10 | 11289017 | C | T | upstream_gene_variant | MODIFIER | c.-3015G>A| |
S63 |
15 | BAA10g09290 | A10 | 11289891 | C | T | upstream_gene_variant | MODIFIER | c.-3889G>A| |
S149 |
16 | BAA10g09290 | A10 | 11290255 | C | T | upstream_gene_variant | MODIFIER | c.-4253G>A| |
S142 |
17 | BAA10g09290 | A10 | 11290524 | C | T | upstream_gene_variant | MODIFIER | c.-4522G>A| |
S123 |
18 | BAA10g09290 | A10 | 11290528 | G | A | upstream_gene_variant | MODIFIER | c.-4526C>T| |
S67 |
19 | BAA10g09290 | A10 | 11290895 | G | A | upstream_gene_variant | MODIFIER | c.-4893C>T| |
S288 |
20 | BAA10g09290 | A10 | 11290947 | G | A | upstream_gene_variant | MODIFIER | c.-4945C>T| |
S192 |