Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g21760 | A06 | 11763553 | G | A | downstream_gene_variant | MODIFIER | c.*3997C>T| |
S139 |
2 | BAA06g21760 | A06 | 11765415 | G | A | downstream_gene_variant | MODIFIER | c.*2135C>T| |
S35 |
3 | BAA06g21760 | A06 | 11766254 | C | T | downstream_gene_variant | MODIFIER | c.*1296G>A| |
S286 |
4 | BAA06g21760 | A06 | 11766674 | C | T | downstream_gene_variant | MODIFIER | c.*876G>A| |
S163 |
5 | BAA06g21760 | A06 | 11766809 | C | T | downstream_gene_variant | MODIFIER | c.*741G>A| |
S56 |
6 | BAA06g21760 | A06 | 11767491 | C | T | downstream_gene_variant | MODIFIER | c.*59G>A| |
S115 |
7 | BAA06g21760 | A06 | 11767597 | G | A | missense_variant | MODERATE | c.1087C>T|p.Pro363Ser |
S219 S72 |
8 | BAA06g21760 | A06 | 11768031 | G | A | missense_variant | MODERATE | c.749C>T|p.Ser250Phe |
S123 |
9 | BAA06g21760 | A06 | 11768259 | T | A | splice_acceptor_variant&intron_variant | HIGH | c.605-2A>T| |
S68 |
10 | BAA06g21760 | A06 | 11768405 | G | A | synonymous_variant | LOW | c.540C>T|p.Thr180Thr |
S203 |
11 | BAA06g21760 | A06 | 11768478 | G | A | missense_variant | MODERATE | c.467C>T|p.Pro156Leu |
S64 |
12 | BAA06g21760 | A06 | 11768873 | G | A | synonymous_variant | LOW | c.72C>T|p.Asp24Asp |
S179 |
13 | BAA06g21760 | A06 | 11769013 | C | T | upstream_gene_variant | MODIFIER | c.-69G>A| |
S236 |
14 | BAA06g21760 | A06 | 11769094 | C | T | upstream_gene_variant | MODIFIER | c.-150G>A| |
S266 |
15 | BAA06g21760 | A06 | 11769782 | G | A | upstream_gene_variant | MODIFIER | c.-838C>T| |
S54 |
16 | BAA06g21760 | A06 | 11771597 | T | G | upstream_gene_variant | MODIFIER | c.-2653A>C| |
S206 S26 |
17 | BAA06g21760 | A06 | 11772275 | G | A | upstream_gene_variant | MODIFIER | c.-3331C>T| |
S233 |
18 | BAA06g21760 | A06 | 11772937 | G | A | upstream_gene_variant | MODIFIER | c.-3993C>T| |
S146 |
19 | BAA06g21760 | A06 | 11773489 | G | A | upstream_gene_variant | MODIFIER | c.-4545C>T| |
S274 |