Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g28320 | A01 | 17368052 | C | T | downstream_gene_variant | MODIFIER | c.*4838G>A| |
S4 |
2 | BAA01g28320 | A01 | 17373067 | C | T | synonymous_variant | LOW | c.1923G>A|p.Glu641Glu |
S303 |
3 | BAA01g28320 | A01 | 17373076 | C | T | stop_gained | HIGH | c.1914G>A|p.Trp638* |
S168 |
4 | BAA01g28320 | A01 | 17373085 | G | A | synonymous_variant | LOW | c.1905C>T|p.Ile635Ile |
S283 |
5 | BAA01g28320 | A01 | 17373147 | C | T | missense_variant | MODERATE | c.1843G>A|p.Ala615Thr |
S167 |
6 | BAA01g28320 | A01 | 17373210 | C | T | missense_variant | MODERATE | c.1780G>A|p.Ala594Thr |
S41 |
7 | BAA01g28320 | A01 | 17373653 | G | A | synonymous_variant | LOW | c.1494C>T|p.Ile498Ile |
S86 |
8 | BAA01g28320 | A01 | 17374277 | G | A | missense_variant | MODERATE | c.1352C>T|p.Ser451Phe |
S121 |
9 | BAA01g28320 | A01 | 17374513 | G | A | synonymous_variant | LOW | c.1116C>T|p.Phe372Phe |
S288 |
10 | BAA01g28320 | A01 | 17374995 | C | T | missense_variant | MODERATE | c.730G>A|p.Glu244Lys |
S186 |
11 | BAA01g28320 | A01 | 17375195 | C | T | missense_variant | MODERATE | c.530G>A|p.Gly177Glu |
S94 |
12 | BAA01g28320 | A01 | 17375603 | C | T | missense_variant | MODERATE | c.241G>A|p.Ala81Thr |
S139 |
13 | BAA01g28320 | A01 | 17375825 | C | T | missense_variant | MODERATE | c.19G>A|p.Asp7Asn |
S272 S284 |
14 | BAA01g28320 | A01 | 17377299 | C | T | upstream_gene_variant | MODIFIER | c.-1456G>A| |
S132 S137 S215 |
15 | BAA01g28320 | A01 | 17377376 | G | A | upstream_gene_variant | MODIFIER | c.-1533C>T| |
S245 |
16 | BAA01g28320 | A01 | 17378001 | G | A | upstream_gene_variant | MODIFIER | c.-2158C>T| |
S109 |
17 | BAA01g28320 | A01 | 17378029 | G | A | upstream_gene_variant | MODIFIER | c.-2186C>T| |
S245 |
18 | BAA01g28320 | A01 | 17378072 | C | T | upstream_gene_variant | MODIFIER | c.-2229G>A| |
S177 |
19 | BAA01g28320 | A01 | 17380420 | C | T | upstream_gene_variant | MODIFIER | c.-4577G>A| |
S122 |