Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46450 | A09 | 51181312 | G | A | upstream_gene_variant | MODIFIER | c.-4064G>A| |
S233 |
2 | BAA09g46450 | A09 | 51181421 | G | C | upstream_gene_variant | MODIFIER | c.-3955G>C| |
S63 |
3 | BAA09g46450 | A09 | 51181521 | G | A | upstream_gene_variant | MODIFIER | c.-3855G>A| |
S128 |
4 | BAA09g46450 | A09 | 51182327 | G | A | upstream_gene_variant | MODIFIER | c.-3049G>A| |
S156 |
5 | BAA09g46450 | A09 | 51183262 | C | T | upstream_gene_variant | MODIFIER | c.-2114C>T| |
S191 |
6 | BAA09g46450 | A09 | 51184852 | G | A | upstream_gene_variant | MODIFIER | c.-524G>A| |
S116 |
7 | BAA09g46450 | A09 | 51185174 | C | T | upstream_gene_variant | MODIFIER | c.-202C>T| |
S163 |
8 | BAA09g46450 | A09 | 51185375 | G | A | upstream_gene_variant | MODIFIER | c.-1G>A| |
S133 |
9 | BAA09g46450 | A09 | 51189490 | G | A | missense_variant | MODERATE | c.469G>A|p.Asp157Asn |
S298 |
10 | BAA09g46450 | A09 | 51189962 | G | A | missense_variant | MODERATE | c.941G>A|p.Arg314His |
S162 |
11 | BAA09g46450 | A09 | 51190482 | G | A | intron_variant | MODIFIER | c.1266+195G>A| |
S15 S3 |
12 | BAA09g46450 | A09 | 51191883 | G | A | intron_variant | MODIFIER | c.1266+1596G>A| |
S23 |
13 | BAA09g46450 | A09 | 51192591 | C | T | intron_variant | MODIFIER | c.1267-1858C>T| |
S296 |
14 | BAA09g46450 | A09 | 51194549 | G | A | downstream_gene_variant | MODIFIER | c.*77G>A| |
S107 |
15 | BAA09g46450 | A09 | 51194872 | C | T | downstream_gene_variant | MODIFIER | c.*400C>T| |
S133 |
16 | BAA09g46450 | A09 | 51196349 | C | T | downstream_gene_variant | MODIFIER | c.*1877C>T| |
S37 |
17 | BAA09g46450 | A09 | 51196905 | G | A | downstream_gene_variant | MODIFIER | c.*2433G>A| |
S148 |