Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g20160 | A09 | 12438351 | C | T | upstream_gene_variant | MODIFIER | c.-4510C>T| |
S192 |
2 | BAA09g20160 | A09 | 12438636 | G | A | upstream_gene_variant | MODIFIER | c.-4225G>A| |
S252 |
3 | BAA09g20160 | A09 | 12439746 | C | T | upstream_gene_variant | MODIFIER | c.-3115C>T| |
S237 |
4 | BAA09g20160 | A09 | 12439990 | G | A | upstream_gene_variant | MODIFIER | c.-2871G>A| |
S162 |
5 | BAA09g20160 | A09 | 12440490 | G | A | upstream_gene_variant | MODIFIER | c.-2371G>A| |
S40 S49 |
6 | BAA09g20160 | A09 | 12440661 | C | T | upstream_gene_variant | MODIFIER | c.-2200C>T| |
S67 |
7 | BAA09g20160 | A09 | 12440811 | G | A | upstream_gene_variant | MODIFIER | c.-2050G>A| |
S73 S91 |
8 | BAA09g20160 | A09 | 12440839 | C | T | upstream_gene_variant | MODIFIER | c.-2022C>T| |
S289 S290 |
9 | BAA09g20160 | A09 | 12441114 | G | A | upstream_gene_variant | MODIFIER | c.-1747G>A| |
S176 |
10 | BAA09g20160 | A09 | 12441295 | G | A | upstream_gene_variant | MODIFIER | c.-1566G>A| |
S203 |
11 | BAA09g20160 | A09 | 12441476 | G | A | upstream_gene_variant | MODIFIER | c.-1385G>A| |
S225 S73 |
12 | BAA09g20160 | A09 | 12441596 | G | A | upstream_gene_variant | MODIFIER | c.-1265G>A| |
S34 |
13 | BAA09g20160 | A09 | 12442395 | C | T | upstream_gene_variant | MODIFIER | c.-466C>T| |
S71 |
14 | BAA09g20160 | A09 | 12442918 | G | A | missense_variant | MODERATE | c.58G>A|p.Glu20Lys |
S193 |
15 | BAA09g20160 | A09 | 12442967 | C | T | missense_variant | MODERATE | c.107C>T|p.Ala36Val |
S94 |
16 | BAA09g20160 | A09 | 12443008 | C | T | missense_variant | MODERATE | c.148C>T|p.Pro50Ser |
S94 |
17 | BAA09g20160 | A09 | 12443311 | G | A | missense_variant | MODERATE | c.371G>A|p.Ser124Asn |
S25 S264 |