Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g12780 | A08 | 11153436 | G | A | upstream_gene_variant | MODIFIER | c.-1078G>A| |
S65 |
2 | BAA08g12780 | A08 | 11153869 | C | T | upstream_gene_variant | MODIFIER | c.-645C>T| |
S152 |
3 | BAA08g12780 | A08 | 11154299 | T | C | upstream_gene_variant | MODIFIER | c.-215T>C| |
S148 S210 S30 S31 |
4 | BAA08g12780 | A08 | 11154436 | C | T | upstream_gene_variant | MODIFIER | c.-78C>T| |
S112 |
5 | BAA08g12780 | A08 | 11154733 | G | A | intron_variant | MODIFIER | c.139+81G>A| |
S20 |
6 | BAA08g12780 | A08 | 11154763 | G | A | intron_variant | MODIFIER | c.139+111G>A| |
S108 |
7 | BAA08g12780 | A08 | 11155213 | G | A | intron_variant | MODIFIER | c.140-177G>A| |
S28 |
8 | BAA08g12780 | A08 | 11155306 | G | A | intron_variant | MODIFIER | c.140-84G>A| |
S131 |
9 | BAA08g12780 | A08 | 11155900 | G | A | missense_variant | MODERATE | c.385G>A|p.Glu129Lys |
S165 |
10 | BAA08g12780 | A08 | 11156215 | C | T | missense_variant | MODERATE | c.700C>T|p.Pro234Ser |
S47 |
11 | BAA08g12780 | A08 | 11156745 | A | T | synonymous_variant | LOW | c.1230A>T|p.Gly410Gly |
S1 S161 S244 |
12 | BAA08g12780 | A08 | 11157089 | G | A | missense_variant | MODERATE | c.1574G>A|p.Gly525Asp |
S181 |
13 | BAA08g12780 | A08 | 11157135 | T | A | missense_variant | MODERATE | c.1620T>A|p.Asn540Lys |
S123 S256 |
14 | BAA08g12780 | A08 | 11157559 | C | T | missense_variant | MODERATE | c.1937C>T|p.Pro646Leu |
S134 |
15 | BAA08g12780 | A08 | 11158418 | G | A | downstream_gene_variant | MODIFIER | c.*144G>A| |
S65 |
16 | BAA08g12780 | A08 | 11159652 | G | A | downstream_gene_variant | MODIFIER | c.*1378G>A| |
S263 |
17 | BAA08g12780 | A08 | 11160523 | G | T | downstream_gene_variant | MODIFIER | c.*2249G>T| |
S305 |
18 | BAA08g12780 | A08 | 11160536 | T | A | downstream_gene_variant | MODIFIER | c.*2262T>A| |
S244 |