Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g20170 | A09 | 12443153 | G | A | upstream_gene_variant | MODIFIER | c.-2634G>A| |
S249 |
2 | BAA09g20170 | A09 | 12444321 | C | T | upstream_gene_variant | MODIFIER | c.-1466C>T| |
S259 |
3 | BAA09g20170 | A09 | 12444338 | G | A | upstream_gene_variant | MODIFIER | c.-1449G>A| |
S78 S83 |
4 | BAA09g20170 | A09 | 12444445 | C | T | upstream_gene_variant | MODIFIER | c.-1342C>T| |
S231 |
5 | BAA09g20170 | A09 | 12444677 | C | T | upstream_gene_variant | MODIFIER | c.-1110C>T| |
S158 |
6 | BAA09g20170 | A09 | 12444869 | C | T | upstream_gene_variant | MODIFIER | c.-918C>T| |
S305 |
7 | BAA09g20170 | A09 | 12444901 | G | A | upstream_gene_variant | MODIFIER | c.-886G>A| |
S172 S217 |
8 | BAA09g20170 | A09 | 12444925 | C | T | upstream_gene_variant | MODIFIER | c.-862C>T| |
S186 |
9 | BAA09g20170 | A09 | 12445011 | G | A | upstream_gene_variant | MODIFIER | c.-776G>A| |
S138 |
10 | BAA09g20170 | A09 | 12445315 | G | A | upstream_gene_variant | MODIFIER | c.-472G>A| |
S201 |
11 | BAA09g20170 | A09 | 12445526 | C | T | upstream_gene_variant | MODIFIER | c.-261C>T| |
S294 |
12 | BAA09g20170 | A09 | 12447899 | C | T | missense_variant | MODERATE | c.1003C>T|p.Pro335Ser |
S36 |
13 | BAA09g20170 | A09 | 12448626 | G | A | synonymous_variant | LOW | c.1575G>A|p.Glu525Glu |
S139 |
14 | BAA09g20170 | A09 | 12448975 | G | A | missense_variant | MODERATE | c.1748G>A|p.Ser583Asn |
S247 |
15 | BAA09g20170 | A09 | 12449204 | C | T | missense_variant | MODERATE | c.1901C>T|p.Thr634Ile |
S108 |
16 | BAA09g20170 | A09 | 12449263 | G | A | missense_variant | MODERATE | c.1960G>A|p.Ala654Thr |
S288 |
17 | BAA09g20170 | A09 | 12453435 | C | T | downstream_gene_variant | MODIFIER | c.*4035C>T| |
S96 |