Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14160 | A10 | 14976510 | G | A | downstream_gene_variant | MODIFIER | c.*704C>T| |
S262 |
2 | BAA10g14160 | A10 | 14976807 | C | T | downstream_gene_variant | MODIFIER | c.*407G>A| |
S211 |
3 | BAA10g14160 | A10 | 14976894 | G | A | downstream_gene_variant | MODIFIER | c.*320C>T| |
S59 |
4 | BAA10g14160 | A10 | 14977679 | C | T | missense_variant | MODERATE | c.1306G>A|p.Asp436Asn |
S68 |
5 | BAA10g14160 | A10 | 14977923 | G | A | synonymous_variant | LOW | c.1062C>T|p.Pro354Pro |
S10 |
6 | BAA10g14160 | A10 | 14978732 | G | A | missense_variant | MODERATE | c.335C>T|p.Thr112Ile |
S90 |
7 | BAA10g14160 | A10 | 14979569 | C | T | upstream_gene_variant | MODIFIER | c.-404G>A| |
S10 |
8 | BAA10g14160 | A10 | 14981045 | G | A | upstream_gene_variant | MODIFIER | c.-1880C>T| |
S286 |
9 | BAA10g14160 | A10 | 14981456 | T | G | upstream_gene_variant | MODIFIER | c.-2291A>C| |
S112 |
10 | BAA10g14160 | A10 | 14982218 | G | A | upstream_gene_variant | MODIFIER | c.-3053C>T| |
S252 |
11 | BAA10g14160 | A10 | 14982297 | C | T | upstream_gene_variant | MODIFIER | c.-3132G>A| |
S308 |
12 | BAA10g14160 | A10 | 14982317 | G | A | upstream_gene_variant | MODIFIER | c.-3152C>T| |
S138 |
13 | BAA10g14160 | A10 | 14982694 | C | T | upstream_gene_variant | MODIFIER | c.-3529G>A| |
S165 S211 S227 |
14 | BAA10g14160 | A10 | 14982781 | G | A | upstream_gene_variant | MODIFIER | c.-3616C>T| |
S25 |
15 | BAA10g14160 | A10 | 14983312 | G | A | upstream_gene_variant | MODIFIER | c.-4147C>T| |
S67 |