Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09220 | A10 | 11247451 | A | T | downstream_gene_variant | MODIFIER | c.*4163T>A| |
S125 |
2 | BAA10g09220 | A10 | 11248054 | C | T | downstream_gene_variant | MODIFIER | c.*3560G>A| |
S20 |
3 | BAA10g09220 | A10 | 11248223 | C | T | downstream_gene_variant | MODIFIER | c.*3391G>A| |
S259 |
4 | BAA10g09220 | A10 | 11251730 | C | T | missense_variant | MODERATE | c.406G>A|p.Asp136Asn |
S20 |
5 | BAA10g09220 | A10 | 11251733 | C | T | missense_variant | MODERATE | c.403G>A|p.Val135Met |
S259 |
6 | BAA10g09220 | A10 | 11251766 | C | T | missense_variant | MODERATE | c.370G>A|p.Glu124Lys |
S70 |
7 | BAA10g09220 | A10 | 11252096 | C | T | missense_variant&splice_region_variant | MODERATE | c.223G>A|p.Val75Ile |
S10 |
8 | BAA10g09220 | A10 | 11252881 | G | A | upstream_gene_variant | MODIFIER | c.-345C>T| |
S13 |
9 | BAA10g09220 | A10 | 11253206 | G | A | upstream_gene_variant | MODIFIER | c.-670C>T| |
S192 |
10 | BAA10g09220 | A10 | 11253213 | G | A | upstream_gene_variant | MODIFIER | c.-677C>T| |
S150 |
11 | BAA10g09220 | A10 | 11253695 | C | T | upstream_gene_variant | MODIFIER | c.-1159G>A| |
S246 |
12 | BAA10g09220 | A10 | 11254192 | C | T | upstream_gene_variant | MODIFIER | c.-1656G>A| |
S235 |
13 | BAA10g09220 | A10 | 11255681 | C | T | upstream_gene_variant | MODIFIER | c.-3145G>A| |
S191 |