Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00980 | A10 | 470442 | C | T | missense_variant | MODERATE | c.426G>A|p.Met142Ile |
S74 |
2 | BAA10g00980 | A10 | 470589 | C | T | synonymous_variant | LOW | c.390G>A|p.Glu130Glu |
S152 |
3 | BAA10g00980 | A10 | 470894 | G | A | missense_variant&splice_region_variant | MODERATE | c.157C>T|p.Arg53Trp |
S96 |
4 | BAA10g00980 | A10 | 471020 | G | A | missense_variant | MODERATE | c.31C>T|p.Pro11Ser |
S295 |
5 | BAA10g00980 | A10 | 471984 | C | T | upstream_gene_variant | MODIFIER | c.-934G>A| |
S84 S93 |
6 | BAA10g00980 | A10 | 472766 | G | A | upstream_gene_variant | MODIFIER | c.-1716C>T| |
S251 |
7 | BAA10g00980 | A10 | 472826 | G | A | upstream_gene_variant | MODIFIER | c.-1776C>T| |
S136 |
8 | BAA10g00980 | A10 | 473170 | C | T | upstream_gene_variant | MODIFIER | c.-2120G>A| |
S87 |