Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g33000 | A09 | 41568901 | C | T | downstream_gene_variant | MODIFIER | c.*2407G>A| |
S245 |
2 | BAA09g33000 | A09 | 41570026 | C | T | downstream_gene_variant | MODIFIER | c.*1282G>A| |
S60 |
3 | BAA09g33000 | A09 | 41571110 | G | A | downstream_gene_variant | MODIFIER | c.*198C>T| |
S65 |
4 | BAA09g33000 | A09 | 41571233 | G | A | downstream_gene_variant | MODIFIER | c.*75C>T| |
S262 |
5 | BAA09g33000 | A09 | 41572254 | C | T | intron_variant | MODIFIER | c.1104+306G>A| |
S247 |
6 | BAA09g33000 | A09 | 41572314 | C | T | intron_variant | MODIFIER | c.1104+246G>A| |
S269 |
7 | BAA09g33000 | A09 | 41572352 | C | T | intron_variant | MODIFIER | c.1104+208G>A| |
S229 |
8 | BAA09g33000 | A09 | 41572466 | C | T | intron_variant | MODIFIER | c.1104+94G>A| |
S69 |
9 | BAA09g33000 | A09 | 41572975 | C | T | splice_region_variant&intron_variant | LOW | c.844+5G>A| |
S109 |
10 | BAA09g33000 | A09 | 41573452 | G | A | synonymous_variant | LOW | c.372C>T|p.Tyr124Tyr |
S194 |
11 | BAA09g33000 | A09 | 41573471 | G | A | missense_variant | MODERATE | c.353C>T|p.Thr118Met |
S156 |
12 | BAA09g33000 | A09 | 41573675 | G | A | missense_variant | MODERATE | c.149C>T|p.Ser50Phe |
S40 S49 |
13 | BAA09g33000 | A09 | 41574046 | G | A | upstream_gene_variant | MODIFIER | c.-223C>T| |
S170 |
14 | BAA09g33000 | A09 | 41574451 | T | A | upstream_gene_variant | MODIFIER | c.-628A>T| |
S239 |
15 | BAA09g33000 | A09 | 41575231 | C | T | upstream_gene_variant | MODIFIER | c.-1408G>A| |
S247 |
16 | BAA09g33000 | A09 | 41575334 | C | T | upstream_gene_variant | MODIFIER | c.-1511G>A| |
S200 S303 |
17 | BAA09g33000 | A09 | 41578044 | C | T | upstream_gene_variant | MODIFIER | c.-4221G>A| |
S278 |