Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29860 | A10 | 22315888 | C | T | missense_variant | MODERATE | c.46C>T|p.Leu16Phe |
S33 |
2 | BAA10g29860 | A10 | 22317650 | C | T | missense_variant | MODERATE | c.1270C>T|p.His424Tyr |
S133 |
3 | BAA10g29860 | A10 | 22317689 | G | A | missense_variant | MODERATE | c.1309G>A|p.Val437Ile |
S228 |
4 | BAA10g29860 | A10 | 22317790 | G | A | synonymous_variant | LOW | c.1410G>A|p.Arg470Arg |
S219 S72 |
5 | BAA10g29860 | A10 | 22317812 | G | A | missense_variant | MODERATE | c.1432G>A|p.Asp478Asn |
S140 S168 S278 S64 |
6 | BAA10g29860 | A10 | 22318550 | C | T | missense_variant | MODERATE | c.2170C>T|p.Pro724Ser |
S187 |
7 | BAA10g29860 | A10 | 22318584 | G | A | missense_variant | MODERATE | c.2204G>A|p.Gly735Glu |
S109 |
8 | BAA10g29860 | A10 | 22318637 | C | T | missense_variant | MODERATE | c.2257C>T|p.Pro753Ser |
S5 |
9 | BAA10g29860 | A10 | 22319216 | C | T | missense_variant | MODERATE | c.2570C>T|p.Ala857Val |
S107 |
10 | BAA10g29860 | A10 | 22319821 | G | A | splice_region_variant&synonymous_variant | LOW | c.2847G>A|p.Gln949Gln |
S179 |
11 | BAA10g29860 | A10 | 22320947 | G | A | missense_variant | MODERATE | c.3370G>A|p.Glu1124Lys |
S263 |
12 | BAA10g29860 | A10 | 22321334 | C | T | downstream_gene_variant | MODIFIER | c.*89C>T| |
S292 |
13 | BAA10g29860 | A10 | 22321704 | G | A | downstream_gene_variant | MODIFIER | c.*459G>A| |
S125 |
14 | BAA10g29860 | A10 | 22321885 | G | A | downstream_gene_variant | MODIFIER | c.*640G>A| |
S75 |