Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02640 | A10 | 1260709 | C | T | upstream_gene_variant | MODIFIER | c.-3706C>T| |
S221 |
2 | BAA10g02640 | A10 | 1261495 | G | A | upstream_gene_variant | MODIFIER | c.-2920G>A| |
S64 |
3 | BAA10g02640 | A10 | 1261504 | G | A | upstream_gene_variant | MODIFIER | c.-2911G>A| |
S151 S263 |
4 | BAA10g02640 | A10 | 1263269 | C | T | upstream_gene_variant | MODIFIER | c.-1146C>T| |
S233 |
5 | BAA10g02640 | A10 | 1263387 | G | A | upstream_gene_variant | MODIFIER | c.-1028G>A| |
S286 |
6 | BAA10g02640 | A10 | 1264121 | G | A | upstream_gene_variant | MODIFIER | c.-294G>A| |
S212 |
7 | BAA10g02640 | A10 | 1264206 | C | T | upstream_gene_variant | MODIFIER | c.-209C>T| |
S25 |
8 | BAA10g02640 | A10 | 1264409 | G | A | upstream_gene_variant | MODIFIER | c.-6G>A| |
S38 |
9 | BAA10g02640 | A10 | 1264642 | G | A | synonymous_variant | LOW | c.228G>A|p.Ala76Ala |
S303 |
10 | BAA10g02640 | A10 | 1265515 | G | A | missense_variant | MODERATE | c.860G>A|p.Gly287Glu |
S178 |
11 | BAA10g02640 | A10 | 1265566 | G | A | missense_variant | MODERATE | c.911G>A|p.Gly304Glu |
S286 |
12 | BAA10g02640 | A10 | 1267836 | G | A | missense_variant | MODERATE | c.1063G>A|p.Gly355Arg |
S218 |
13 | BAA10g02640 | A10 | 1268242 | G | A | splice_region_variant&synonymous_variant | LOW | c.1293G>A|p.Lys431Lys |
S289 |