Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g18740 | A06 | 9581544 | C | T | upstream_gene_variant | MODIFIER | c.-3983C>T| |
S121 |
2 | BAA06g18740 | A06 | 9582322 | C | T | upstream_gene_variant | MODIFIER | c.-3205C>T| |
S266 |
3 | BAA06g18740 | A06 | 9582375 | C | T | upstream_gene_variant | MODIFIER | c.-3152C>T| |
S70 |
4 | BAA06g18740 | A06 | 9582458 | G | A | upstream_gene_variant | MODIFIER | c.-3069G>A| |
S169 |
5 | BAA06g18740 | A06 | 9582466 | C | T | upstream_gene_variant | MODIFIER | c.-3061C>T| |
S159 S243 |
6 | BAA06g18740 | A06 | 9582546 | C | T | upstream_gene_variant | MODIFIER | c.-2981C>T| |
S293 |
7 | BAA06g18740 | A06 | 9582994 | C | T | upstream_gene_variant | MODIFIER | c.-2533C>T| |
S121 |
8 | BAA06g18740 | A06 | 9583373 | T | A | upstream_gene_variant | MODIFIER | c.-2154T>A| |
S77 S82 |
9 | BAA06g18740 | A06 | 9585970 | G | A | synonymous_variant | LOW | c.444G>A|p.Glu148Glu |
S206 S26 |
10 | BAA06g18740 | A06 | 9586573 | G | A | missense_variant | MODERATE | c.1047G>A|p.Met349Ile |
S216 |
11 | BAA06g18740 | A06 | 9586807 | G | A | stop_gained | HIGH | c.1281G>A|p.Trp427* |
S50 |
12 | BAA06g18740 | A06 | 9587052 | C | T | missense_variant | MODERATE | c.1526C>T|p.Ser509Phe |
S289 S290 |
13 | BAA06g18740 | A06 | 9590304 | G | A | downstream_gene_variant | MODIFIER | c.*2879G>A| |
S308 |