Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g36620 | A05 | 36574079 | G | A | missense_variant | MODERATE | c.4G>A|p.Ala2Thr |
S74 |
2 | BAA05g36620 | A05 | 36574305 | G | A | synonymous_variant | LOW | c.72G>A|p.Lys24Lys |
S149 |
3 | BAA05g36620 | A05 | 36574613 | C | T | missense_variant | MODERATE | c.380C>T|p.Thr127Ile |
S294 |
4 | BAA05g36620 | A05 | 36574636 | C | T | missense_variant | MODERATE | c.403C>T|p.Pro135Ser |
S187 |
5 | BAA05g36620 | A05 | 36574774 | G | A | missense_variant | MODERATE | c.541G>A|p.Asp181Asn |
S74 |
6 | BAA05g36620 | A05 | 36575102 | C | T | missense_variant | MODERATE | c.869C>T|p.Ala290Val |
S73 |
7 | BAA05g36620 | A05 | 36575641 | C | T | missense_variant | MODERATE | c.1408C>T|p.Pro470Ser |
S206 S26 |
8 | BAA05g36620 | A05 | 36575917 | C | T | missense_variant | MODERATE | c.1684C>T|p.Pro562Ser |
S157 |
9 | BAA05g36620 | A05 | 36576525 | G | A | intron_variant | MODIFIER | c.1843-206G>A| |
S250 |
10 | BAA05g36620 | A05 | 36576584 | C | T | intron_variant | MODIFIER | c.1843-147C>T| |
S82 S92 |
11 | BAA05g36620 | A05 | 36576859 | G | A | synonymous_variant | LOW | c.1971G>A|p.Lys657Lys |
S138 |
12 | BAA05g36620 | A05 | 36577318 | C | T | synonymous_variant | LOW | c.2430C>T|p.Leu810Leu |
S277 |
13 | BAA05g36620 | A05 | 36577503 | C | T | missense_variant | MODERATE | c.2615C>T|p.Ser872Phe |
S42 |
14 | BAA05g36620 | A05 | 36577716 | C | T | missense_variant | MODERATE | c.2828C>T|p.Thr943Ile |
S286 |
15 | BAA05g36620 | A05 | 36577951 | C | T | synonymous_variant | LOW | c.3063C>T|p.Asn1021Asn |
S157 |