Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g27050 | A05 | 31483524 | G | A | downstream_gene_variant | MODIFIER | c.*1147C>T| |
S44 |
2 | BAA05g27050 | A05 | 31485991 | G | A | splice_region_variant&intron_variant | LOW | c.1907+7C>T| |
S13 |
3 | BAA05g27050 | A05 | 31485998 | C | T | missense_variant&splice_region_variant | MODERATE | c.1907G>A|p.Arg636Lys |
S262 |
4 | BAA05g27050 | A05 | 31486087 | G | A | splice_region_variant&intron_variant | LOW | c.1821-3C>T| |
S247 |
5 | BAA05g27050 | A05 | 31486522 | G | A | synonymous_variant | LOW | c.1659C>T|p.Pro553Pro |
S67 |
6 | BAA05g27050 | A05 | 31486728 | G | A | synonymous_variant | LOW | c.1554C>T|p.Ala518Ala |
S133 |
7 | BAA05g27050 | A05 | 31488310 | C | T | splice_region_variant&intron_variant | LOW | c.1047+5G>A| |
S276 |
8 | BAA05g27050 | A05 | 31488332 | C | T | missense_variant | MODERATE | c.1030G>A|p.Asp344Asn |
S19 |
9 | BAA05g27050 | A05 | 31488967 | G | A | intron_variant | MODIFIER | c.844-103C>T| |
S187 |
10 | BAA05g27050 | A05 | 31490603 | C | T | intron_variant | MODIFIER | c.317+48G>A| |
S189 |
11 | BAA05g27050 | A05 | 31490806 | C | T | synonymous_variant | LOW | c.237G>A|p.Gln79Gln |
S250 |
12 | BAA05g27050 | A05 | 31490985 | C | T | intron_variant | MODIFIER | c.164-106G>A| |
S36 |
13 | BAA05g27050 | A05 | 31491566 | G | A | intron_variant | MODIFIER | c.36+155C>T| |
S293 |
14 | BAA05g27050 | A05 | 31492867 | C | T | upstream_gene_variant | MODIFIER | c.-1111G>A| |
S294 |
15 | BAA05g27050 | A05 | 31492926 | G | A | upstream_gene_variant | MODIFIER | c.-1170C>T| |
S80 |
16 | BAA05g27050 | A05 | 31493159 | G | A | upstream_gene_variant | MODIFIER | c.-1403C>T| |
S41 |
17 | BAA05g27050 | A05 | 31493733 | G | A | upstream_gene_variant | MODIFIER | c.-1977C>T| |
S133 |
18 | BAA05g27050 | A05 | 31496049 | G | A | upstream_gene_variant | MODIFIER | c.-4293C>T| |
S174 S241 S27 S39 |