Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g59410 | A03 | 29769609 | G | A | upstream_gene_variant | MODIFIER | c.-4456G>A| |
S308 |
2 | BAA03g59410 | A03 | 29770831 | C | T | upstream_gene_variant | MODIFIER | c.-3234C>T| |
S34 |
3 | BAA03g59410 | A03 | 29770848 | G | A | upstream_gene_variant | MODIFIER | c.-3217G>A| |
S242 |
4 | BAA03g59410 | A03 | 29771018 | G | A | upstream_gene_variant | MODIFIER | c.-3047G>A| |
S135 |
5 | BAA03g59410 | A03 | 29771166 | C | T | upstream_gene_variant | MODIFIER | c.-2899C>T| |
S61 |
6 | BAA03g59410 | A03 | 29773713 | C | T | upstream_gene_variant | MODIFIER | c.-352C>T| |
S33 |
7 | BAA03g59410 | A03 | 29775056 | C | T | missense_variant | MODERATE | c.992C>T|p.Ser331Phe |
S13 |
8 | BAA03g59410 | A03 | 29775171 | T | A | synonymous_variant | LOW | c.1107T>A|p.Ala369Ala |
S51 |
9 | BAA03g59410 | A03 | 29775333 | C | T | synonymous_variant | LOW | c.1269C>T|p.Val423Val |
S180 |
10 | BAA03g59410 | A03 | 29775934 | G | A | missense_variant | MODERATE | c.1870G>A|p.Asp624Asn |
S167 |
11 | BAA03g59410 | A03 | 29775942 | G | A | synonymous_variant | LOW | c.1878G>A|p.Arg626Arg |
S272 |
12 | BAA03g59410 | A03 | 29775969 | G | A | synonymous_variant | LOW | c.1905G>A|p.Glu635Glu |
S170 |
13 | BAA03g59410 | A03 | 29776168 | G | A | missense_variant | MODERATE | c.2104G>A|p.Gly702Arg |
S146 |
14 | BAA03g59410 | A03 | 29776424 | C | T | missense_variant | MODERATE | c.2360C>T|p.Ser787Leu |
S241 |