Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g59440 | A03 | 29786347 | G | A | missense_variant | MODERATE | c.3026C>T|p.Ser1009Leu |
S146 |
2 | BAA03g59440 | A03 | 29786916 | C | T | synonymous_variant | LOW | c.2538G>A|p.Arg846Arg |
S201 |
3 | BAA03g59440 | A03 | 29787041 | C | T | missense_variant | MODERATE | c.2413G>A|p.Ala805Thr |
S142 |
4 | BAA03g59440 | A03 | 29787399 | C | T | synonymous_variant | LOW | c.2130G>A|p.Glu710Glu |
S211 S227 |
5 | BAA03g59440 | A03 | 29787519 | C | T | missense_variant | MODERATE | c.2074G>A|p.Ala692Thr |
S277 |
6 | BAA03g59440 | A03 | 29787907 | G | A | synonymous_variant | LOW | c.1767C>T|p.Cys589Cys |
S25 |
7 | BAA03g59440 | A03 | 29788695 | G | A | synonymous_variant | LOW | c.1236C>T|p.Phe412Phe |
S282 |
8 | BAA03g59440 | A03 | 29789194 | C | T | missense_variant | MODERATE | c.898G>A|p.Asp300Asn |
S42 |
9 | BAA03g59440 | A03 | 29790240 | G | A | splice_region_variant&intron_variant | LOW | c.278-3C>T| |
S259 |
10 | BAA03g59440 | A03 | 29791388 | G | A | upstream_gene_variant | MODIFIER | c.-571C>T| |
S168 |
11 | BAA03g59440 | A03 | 29791521 | C | T | upstream_gene_variant | MODIFIER | c.-704G>A| |
S138 |
12 | BAA03g59440 | A03 | 29791657 | C | T | upstream_gene_variant | MODIFIER | c.-840G>A| |
S103 |
13 | BAA03g59440 | A03 | 29793187 | G | A | upstream_gene_variant | MODIFIER | c.-2370C>T| |
S84 S93 |
14 | BAA03g59440 | A03 | 29793582 | C | T | upstream_gene_variant | MODIFIER | c.-2765G>A| |
S173 |
15 | BAA03g59440 | A03 | 29794594 | C | T | upstream_gene_variant | MODIFIER | c.-3777G>A| |
S202 |
16 | BAA03g59440 | A03 | 29794628 | C | T | upstream_gene_variant | MODIFIER | c.-3811G>A| |
S84 S93 |