Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37040 | A02 | 31671529 | C | T | downstream_gene_variant | MODIFIER | c.*115G>A| |
S249 |
2 | BAA02g37040 | A02 | 31671874 | C | T | missense_variant | MODERATE | c.2185G>A|p.Gly729Ser |
S255 |
3 | BAA02g37040 | A02 | 31673609 | C | T | intron_variant | MODIFIER | c.2099-1649G>A| |
S267 |
4 | BAA02g37040 | A02 | 31673743 | C | T | intron_variant | MODIFIER | c.2099-1783G>A| |
S3 |
5 | BAA02g37040 | A02 | 31673772 | C | T | intron_variant | MODIFIER | c.2099-1812G>A| |
S25 S264 |
6 | BAA02g37040 | A02 | 31674803 | C | T | intron_variant | MODIFIER | c.2099-2843G>A| |
S115 S276 |
7 | BAA02g37040 | A02 | 31675183 | C | T | intron_variant | MODIFIER | c.2099-3223G>A| |
S255 |
8 | BAA02g37040 | A02 | 31676142 | C | T | intron_variant | MODIFIER | c.2098+2416G>A| |
S18 |
9 | BAA02g37040 | A02 | 31676665 | G | A | intron_variant | MODIFIER | c.2098+1893C>T| |
S90 |
10 | BAA02g37040 | A02 | 31678338 | G | A | intron_variant | MODIFIER | c.2098+220C>T| |
S164 |
11 | BAA02g37040 | A02 | 31678378 | G | A | intron_variant | MODIFIER | c.2098+180C>T| |
S146 |
12 | BAA02g37040 | A02 | 31678473 | G | A | intron_variant | MODIFIER | c.2098+85C>T| |
S191 |
13 | BAA02g37040 | A02 | 31679238 | C | T | synonymous_variant | LOW | c.1608G>A|p.Gly536Gly |
S107 |
14 | BAA02g37040 | A02 | 31680125 | C | T | intron_variant | MODIFIER | c.1526+53G>A| |
S216 |
15 | BAA02g37040 | A02 | 31680238 | C | T | missense_variant | MODERATE | c.1466G>A|p.Ser489Asn |
S289 S290 |
16 | BAA02g37040 | A02 | 31680543 | G | A | synonymous_variant | LOW | c.1248C>T|p.His416His |
S67 |
17 | BAA02g37040 | A02 | 31680553 | C | T | missense_variant | MODERATE | c.1238G>A|p.Arg413Gln |
S165 |
18 | BAA02g37040 | A02 | 31680560 | C | T | missense_variant | MODERATE | c.1231G>A|p.Gly411Arg |
S267 |
19 | BAA02g37040 | A02 | 31680714 | C | T | splice_region_variant&synonymous_variant | LOW | c.1077G>A|p.Arg359Arg |
S173 |
20 | BAA02g37040 | A02 | 31680830 | C | T | missense_variant | MODERATE | c.1066G>A|p.Asp356Asn |
S149 |
21 | BAA02g37040 | A02 | 31680883 | C | T | intron_variant | MODIFIER | c.1028-15G>A| |
S139 |
22 | BAA02g37040 | A02 | 31681601 | C | T | synonymous_variant | LOW | c.888G>A|p.Arg296Arg |
S6 |
23 | BAA02g37040 | A02 | 31681622 | C | T | synonymous_variant | LOW | c.867G>A|p.Glu289Glu |
S250 |
24 | BAA02g37040 | A02 | 31682306 | C | T | missense_variant | MODERATE | c.373G>A|p.Asp125Asn |
S303 |
25 | BAA02g37040 | A02 | 31682307 | C | T | synonymous_variant | LOW | c.372G>A|p.Lys124Lys |
S185 |