Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15740 | A10 | 15984876 | C | T | synonymous_variant | LOW | c.519C>T|p.Pro173Pro |
S305 |
2 | BAA10g15740 | A10 | 15985243 | G | A | splice_donor_variant&intron_variant | HIGH | c.885+1G>A| |
S111 |
3 | BAA10g15740 | A10 | 15985516 | C | T | missense_variant | MODERATE | c.1073C>T|p.Pro358Leu |
S242 |
4 | BAA10g15740 | A10 | 15985577 | C | T | synonymous_variant | LOW | c.1134C>T|p.Ser378Ser |
S298 |
5 | BAA10g15740 | A10 | 15986035 | C | T | synonymous_variant | LOW | c.1515C>T|p.Thr505Thr |
S210 S225 |
6 | BAA10g15740 | A10 | 15986288 | C | T | missense_variant | MODERATE | c.1702C>T|p.Pro568Ser |
S19 |
7 | BAA10g15740 | A10 | 15986438 | C | T | splice_region_variant&intron_variant | LOW | c.1755-5C>T| |
S199 |
8 | BAA10g15740 | A10 | 15986492 | G | A | missense_variant | MODERATE | c.1804G>A|p.Glu602Lys |
S69 |
9 | BAA10g15740 | A10 | 15986679 | G | A | synonymous_variant | LOW | c.1884G>A|p.Glu628Glu |
S291 |
10 | BAA10g15740 | A10 | 15986698 | C | T | missense_variant | MODERATE | c.1903C>T|p.Leu635Phe |
S60 |
11 | BAA10g15740 | A10 | 15986775 | C | T | synonymous_variant | LOW | c.1980C>T|p.Asp660Asp |
S124 |
12 | BAA10g15740 | A10 | 15987168 | C | T | synonymous_variant | LOW | c.2373C>T|p.Pro791Pro |
S301 S304 |