Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g29120 | A01 | 18330740 | C | T | upstream_gene_variant | MODIFIER | c.-4805C>T| |
S50 |
2 | BAA01g29120 | A01 | 18331249 | G | A | upstream_gene_variant | MODIFIER | c.-4296G>A| |
S181 |
3 | BAA01g29120 | A01 | 18337209 | C | T | missense_variant | MODERATE | c.880C>T|p.Leu294Phe |
S155 S211 |
4 | BAA01g29120 | A01 | 18337525 | C | T | synonymous_variant | LOW | c.996C>T|p.Ser332Ser |
S15 S2 S3 S34 S4 S6 |
5 | BAA01g29120 | A01 | 18337979 | G | A | intron_variant | MODIFIER | c.1335+115G>A| |
S252 |
6 | BAA01g29120 | A01 | 18338112 | A | T | intron_variant | MODIFIER | c.1336-90A>T| |
S86 |
7 | BAA01g29120 | A01 | 18338120 | C | T | intron_variant | MODIFIER | c.1336-82C>T| |
S134 |
8 | BAA01g29120 | A01 | 18338173 | C | T | intron_variant | MODIFIER | c.1336-29C>T| |
S242 |
9 | BAA01g29120 | A01 | 18339980 | C | T | synonymous_variant | LOW | c.2481C>T|p.Ile827Ile |
S219 S72 |
10 | BAA01g29120 | A01 | 18340041 | G | A | missense_variant | MODERATE | c.2542G>A|p.Asp848Asn |
S246 |
11 | BAA01g29120 | A01 | 18340653 | G | A | intron_variant | MODIFIER | c.2936+97G>A| |
S100 |
12 | BAA01g29120 | A01 | 18341051 | C | T | intron_variant | MODIFIER | c.2937-262C>T| |
S120 |
13 | BAA01g29120 | A01 | 18341142 | G | A | intron_variant | MODIFIER | c.2937-171G>A| |
S161 |
14 | BAA01g29120 | A01 | 18341354 | G | A | missense_variant | MODERATE | c.2978G>A|p.Gly993Glu |
S281 |
15 | BAA01g29120 | A01 | 18342418 | T | G | missense_variant | MODERATE | c.3750T>G|p.Asp1250Glu |
S105 S108 S270 |
16 | BAA01g29120 | A01 | 18343022 | G | A | intron_variant | MODIFIER | c.3902+37G>A| |
S176 |
17 | BAA01g29120 | A01 | 18343478 | G | A | synonymous_variant | LOW | c.3984G>A|p.Leu1328Leu |
S187 |
18 | BAA01g29120 | A01 | 18343564 | G | A | missense_variant | MODERATE | c.4070G>A|p.Arg1357Lys |
S87 |
19 | BAA01g29120 | A01 | 18343700 | G | A | synonymous_variant | LOW | c.4206G>A|p.Glu1402Glu |
S263 |
20 | BAA01g29120 | A01 | 18343916 | T | G | missense_variant | MODERATE | c.4422T>G|p.His1474Gln |
S164 |
21 | BAA01g29120 | A01 | 18344737 | C | T | missense_variant | MODERATE | c.5243C>T|p.Ser1748Phe |
S240 |
22 | BAA01g29120 | A01 | 18344835 | C | T | splice_region_variant&intron_variant | LOW | c.5269-5C>T| |
S170 |
23 | BAA01g29120 | A01 | 18345564 | C | T | missense_variant | MODERATE | c.5911C>T|p.Pro1971Ser |
S80 |
24 | BAA01g29120 | A01 | 18345839 | C | T | intron_variant | MODIFIER | c.6074+27C>T| |
S142 |
25 | BAA01g29120 | A01 | 18346489 | G | A | intron_variant | MODIFIER | c.6376-152G>A| |
S121 |