Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g20180 | A06 | 10593117 | G | A | upstream_gene_variant | MODIFIER | c.-4585G>A| |
S283 |
2 | BAA06g20180 | A06 | 10593145 | C | T | upstream_gene_variant | MODIFIER | c.-4557C>T| |
S296 |
3 | BAA06g20180 | A06 | 10593285 | A | T | upstream_gene_variant | MODIFIER | c.-4417A>T| |
S292 S31 |
4 | BAA06g20180 | A06 | 10594654 | G | A | upstream_gene_variant | MODIFIER | c.-3048G>A| |
S302 |
5 | BAA06g20180 | A06 | 10595385 | G | A | upstream_gene_variant | MODIFIER | c.-2317G>A| |
S54 |
6 | BAA06g20180 | A06 | 10596481 | C | T | upstream_gene_variant | MODIFIER | c.-1221C>T| |
S259 |
7 | BAA06g20180 | A06 | 10596529 | C | T | upstream_gene_variant | MODIFIER | c.-1173C>T| |
S104 S52 |
8 | BAA06g20180 | A06 | 10597188 | C | T | upstream_gene_variant | MODIFIER | c.-514C>T| |
S127 |
9 | BAA06g20180 | A06 | 10597705 | G | A | missense_variant | MODERATE | c.4G>A|p.Asp2Asn |
S128 |
10 | BAA06g20180 | A06 | 10598050 | C | T | missense_variant | MODERATE | c.349C>T|p.Leu117Phe |
S303 |
11 | BAA06g20180 | A06 | 10598684 | C | T | synonymous_variant | LOW | c.523C>T|p.Leu175Leu |
S293 |
12 | BAA06g20180 | A06 | 10598725 | C | T | synonymous_variant | LOW | c.564C>T|p.Phe188Phe |
S17 |
13 | BAA06g20180 | A06 | 10599071 | G | A | missense_variant | MODERATE | c.811G>A|p.Val271Ile |
S246 |