Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g23530 | A06 | 13784266 | C | T | downstream_gene_variant | MODIFIER | c.*4989G>A| |
S68 |
2 | BAA06g23530 | A06 | 13784287 | G | A | downstream_gene_variant | MODIFIER | c.*4968C>T| |
S13 |
3 | BAA06g23530 | A06 | 13784517 | G | A | downstream_gene_variant | MODIFIER | c.*4738C>T| |
S38 |
4 | BAA06g23530 | A06 | 13785728 | C | T | downstream_gene_variant | MODIFIER | c.*3527G>A| |
S256 |
5 | BAA06g23530 | A06 | 13786095 | C | T | downstream_gene_variant | MODIFIER | c.*3160G>A| |
S68 |
6 | BAA06g23530 | A06 | 13787820 | G | A | downstream_gene_variant | MODIFIER | c.*1435C>T| |
S50 |
7 | BAA06g23530 | A06 | 13788734 | C | T | downstream_gene_variant | MODIFIER | c.*521G>A| |
S277 |
8 | BAA06g23530 | A06 | 13789685 | C | T | intron_variant | MODIFIER | c.1177+34G>A| |
S251 |
9 | BAA06g23530 | A06 | 13790142 | G | A | intron_variant | MODIFIER | c.882-50C>T| |
S47 |
10 | BAA06g23530 | A06 | 13791029 | G | A | missense_variant | MODERATE | c.256C>T|p.Leu86Phe |
S152 |
11 | BAA06g23530 | A06 | 13791031 | C | T | missense_variant | MODERATE | c.254G>A|p.Gly85Asp |
S162 |
12 | BAA06g23530 | A06 | 13792312 | G | A | upstream_gene_variant | MODIFIER | c.-965C>T| |
S188 |
13 | BAA06g23530 | A06 | 13792504 | C | T | upstream_gene_variant | MODIFIER | c.-1157G>A| |
S68 |
14 | BAA06g23530 | A06 | 13793029 | C | T | upstream_gene_variant | MODIFIER | c.-1682G>A| |
S298 |
15 | BAA06g23530 | A06 | 13793154 | G | A | upstream_gene_variant | MODIFIER | c.-1807C>T| |
S256 |
16 | BAA06g23530 | A06 | 13793225 | G | A | upstream_gene_variant | MODIFIER | c.-1878C>T| |
S184 |