Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g04430 | A06 | 2479456 | C | T | upstream_gene_variant | MODIFIER | c.-1150C>T| |
S17 |
2 | BAA06g04430 | A06 | 2479555 | G | A | upstream_gene_variant | MODIFIER | c.-1051G>A| |
S272 |
3 | BAA06g04430 | A06 | 2479739 | C | T | upstream_gene_variant | MODIFIER | c.-867C>T| |
S171 |
4 | BAA06g04430 | A06 | 2480113 | G | A | upstream_gene_variant | MODIFIER | c.-493G>A| |
S308 |
5 | BAA06g04430 | A06 | 2480330 | C | T | upstream_gene_variant | MODIFIER | c.-276C>T| |
S228 |
6 | BAA06g04430 | A06 | 2481007 | C | T | intron_variant | MODIFIER | c.268+35C>T| |
S279 |
7 | BAA06g04430 | A06 | 2481015 | G | A | intron_variant | MODIFIER | c.268+43G>A| |
S71 |
8 | BAA06g04430 | A06 | 2481304 | C | T | intron_variant | MODIFIER | c.269-27C>T| |
S250 |
9 | BAA06g04430 | A06 | 2481463 | C | T | missense_variant | MODERATE | c.401C>T|p.Pro134Leu |
S259 |
10 | BAA06g04430 | A06 | 2481765 | C | T | missense_variant | MODERATE | c.598C>T|p.Leu200Phe |
S53 |
11 | BAA06g04430 | A06 | 2483477 | G | A | missense_variant | MODERATE | c.1324G>A|p.Glu442Lys |
S294 |
12 | BAA06g04430 | A06 | 2484594 | C | T | intron_variant | MODIFIER | c.1659+52C>T| |
S200 |
13 | BAA06g04430 | A06 | 2484666 | C | T | intron_variant | MODIFIER | c.1659+124C>T| |
S167 |
14 | BAA06g04430 | A06 | 2485215 | C | T | intron_variant | MODIFIER | c.1736-84C>T| |
S273 |
15 | BAA06g04430 | A06 | 2489468 | C | T | missense_variant | MODERATE | c.3313C>T|p.His1105Tyr |
S269 |
16 | BAA06g04430 | A06 | 2489745 | G | A | missense_variant | MODERATE | c.3512G>A|p.Ser1171Asn |
S201 S241 |