Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g22940 | A10 | 19512324 | G | A | upstream_gene_variant | MODIFIER | c.-4272G>A| |
S216 |
2 | BAA10g22940 | A10 | 19512845 | G | A | upstream_gene_variant | MODIFIER | c.-3751G>A| |
S298 |
3 | BAA10g22940 | A10 | 19512864 | G | A | upstream_gene_variant | MODIFIER | c.-3732G>A| |
S9 |
4 | BAA10g22940 | A10 | 19513136 | G | A | upstream_gene_variant | MODIFIER | c.-3460G>A| |
S59 |
5 | BAA10g22940 | A10 | 19513838 | G | A | upstream_gene_variant | MODIFIER | c.-2758G>A| |
S55 |
6 | BAA10g22940 | A10 | 19513840 | G | A | upstream_gene_variant | MODIFIER | c.-2756G>A| |
S208 S219 |
7 | BAA10g22940 | A10 | 19514024 | G | A | upstream_gene_variant | MODIFIER | c.-2572G>A| |
S15 |
8 | BAA10g22940 | A10 | 19515794 | C | T | upstream_gene_variant | MODIFIER | c.-802C>T| |
S86 |
9 | BAA10g22940 | A10 | 19515801 | G | A | upstream_gene_variant | MODIFIER | c.-795G>A| |
S138 |
10 | BAA10g22940 | A10 | 19516411 | C | T | upstream_gene_variant | MODIFIER | c.-185C>T| |
S10 |
11 | BAA10g22940 | A10 | 19517041 | C | T | missense_variant | MODERATE | c.446C>T|p.Pro149Leu |
S96 |
12 | BAA10g22940 | A10 | 19519507 | G | A | downstream_gene_variant | MODIFIER | c.*2339G>A| |
S9 |
13 | BAA10g22940 | A10 | 19520342 | G | A | downstream_gene_variant | MODIFIER | c.*3174G>A| |
S216 |
14 | BAA10g22940 | A10 | 19521517 | C | T | downstream_gene_variant | MODIFIER | c.*4349C>T| |
S39 |
15 | BAA10g22940 | A10 | 19521907 | C | T | downstream_gene_variant | MODIFIER | c.*4739C>T| |
S262 |
16 | BAA10g22940 | A10 | 19521941 | C | T | downstream_gene_variant | MODIFIER | c.*4773C>T| |
S11 |