Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g04380 | A08 | 3170384 | C | T | upstream_gene_variant | MODIFIER | c.-4178C>T| |
S216 |
2 | BAA08g04380 | A08 | 3170414 | G | A | upstream_gene_variant | MODIFIER | c.-4148G>A| |
S188 |
3 | BAA08g04380 | A08 | 3170649 | G | A | upstream_gene_variant | MODIFIER | c.-3913G>A| |
S94 |
4 | BAA08g04380 | A08 | 3170666 | C | T | upstream_gene_variant | MODIFIER | c.-3896C>T| |
S67 |
5 | BAA08g04380 | A08 | 3170670 | C | T | upstream_gene_variant | MODIFIER | c.-3892C>T| |
S268 |
6 | BAA08g04380 | A08 | 3171112 | C | T | upstream_gene_variant | MODIFIER | c.-3450C>T| |
S104 S52 |
7 | BAA08g04380 | A08 | 3171493 | G | T | upstream_gene_variant | MODIFIER | c.-3069G>T| |
S226 |
8 | BAA08g04380 | A08 | 3171550 | G | A | upstream_gene_variant | MODIFIER | c.-3012G>A| |
S58 |
9 | BAA08g04380 | A08 | 3171695 | G | A | upstream_gene_variant | MODIFIER | c.-2867G>A| |
S288 |
10 | BAA08g04380 | A08 | 3172112 | C | T | upstream_gene_variant | MODIFIER | c.-2450C>T| |
S293 |
11 | BAA08g04380 | A08 | 3173298 | G | A | upstream_gene_variant | MODIFIER | c.-1264G>A| |
S18 |
12 | BAA08g04380 | A08 | 3175203 | C | T | splice_region_variant&intron_variant | LOW | c.291+7C>T| |
S270 |
13 | BAA08g04380 | A08 | 3175542 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.412-1G>A| |
S221 |
14 | BAA08g04380 | A08 | 3175770 | G | A | missense_variant | MODERATE | c.541G>A|p.Glu181Lys |
S264 |
15 | BAA08g04380 | A08 | 3177046 | C | T | stop_gained | HIGH | c.1141C>T|p.Arg381* |
S140 |