Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01830 | A10 | 878836 | C | T | upstream_gene_variant | MODIFIER | c.-4757C>T| |
S196 |
2 | BAA10g01830 | A10 | 878946 | G | A | upstream_gene_variant | MODIFIER | c.-4647G>A| |
S283 |
3 | BAA10g01830 | A10 | 879557 | G | A | upstream_gene_variant | MODIFIER | c.-4036G>A| |
S156 |
4 | BAA10g01830 | A10 | 879678 | G | A | upstream_gene_variant | MODIFIER | c.-3915G>A| |
S208 |
5 | BAA10g01830 | A10 | 879756 | G | A | upstream_gene_variant | MODIFIER | c.-3837G>A| |
S15 S3 |
6 | BAA10g01830 | A10 | 880987 | G | A | upstream_gene_variant | MODIFIER | c.-2606G>A| |
S302 |
7 | BAA10g01830 | A10 | 881155 | G | A | upstream_gene_variant | MODIFIER | c.-2438G>A| |
S171 |
8 | BAA10g01830 | A10 | 881230 | G | A | upstream_gene_variant | MODIFIER | c.-2363G>A| |
S268 |
9 | BAA10g01830 | A10 | 881717 | G | A | upstream_gene_variant | MODIFIER | c.-1876G>A| |
S292 |
10 | BAA10g01830 | A10 | 881989 | G | A | upstream_gene_variant | MODIFIER | c.-1604G>A| |
S38 |
11 | BAA10g01830 | A10 | 882244 | G | A | upstream_gene_variant | MODIFIER | c.-1349G>A| |
S16 |
12 | BAA10g01830 | A10 | 882503 | G | A | upstream_gene_variant | MODIFIER | c.-1090G>A| |
S9 |
13 | BAA10g01830 | A10 | 883587 | G | A | upstream_gene_variant | MODIFIER | c.-6G>A| |
S32 |
14 | BAA10g01830 | A10 | 883860 | G | A | missense_variant | MODERATE | c.155G>A|p.Gly52Glu |
S57 |
15 | BAA10g01830 | A10 | 883904 | G | A | missense_variant | MODERATE | c.199G>A|p.Asp67Asn |
S250 |
16 | BAA10g01830 | A10 | 884223 | G | A | missense_variant | MODERATE | c.215G>A|p.Gly72Glu |
S251 |
17 | BAA10g01830 | A10 | 887613 | A | G | downstream_gene_variant | MODIFIER | c.*2775A>G| |
S231 |