Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g13250 | A04 | 18708948 | C | T | upstream_gene_variant | MODIFIER | c.-4985C>T| |
S67 |
2 | BAA04g13250 | A04 | 18709427 | G | A | upstream_gene_variant | MODIFIER | c.-4506G>A| |
S40 S49 |
3 | BAA04g13250 | A04 | 18709919 | C | T | upstream_gene_variant | MODIFIER | c.-4014C>T| |
S18 |
4 | BAA04g13250 | A04 | 18710443 | G | A | upstream_gene_variant | MODIFIER | c.-3490G>A| |
S211 |
5 | BAA04g13250 | A04 | 18710475 | C | T | upstream_gene_variant | MODIFIER | c.-3458C>T| |
S202 |
6 | BAA04g13250 | A04 | 18712849 | G | A | upstream_gene_variant | MODIFIER | c.-1084G>A| |
S262 |
7 | BAA04g13250 | A04 | 18713276 | C | T | upstream_gene_variant | MODIFIER | c.-657C>T| |
S232 |
8 | BAA04g13250 | A04 | 18714568 | G | A | synonymous_variant | LOW | c.636G>A|p.Pro212Pro |
S144 |
9 | BAA04g13250 | A04 | 18714674 | C | T | missense_variant | MODERATE | c.742C>T|p.Pro248Ser |
S276 |
10 | BAA04g13250 | A04 | 18715349 | G | A | missense_variant | MODERATE | c.991G>A|p.Ala331Thr |
S162 |
11 | BAA04g13250 | A04 | 18715491 | G | A | missense_variant | MODERATE | c.1133G>A|p.Gly378Glu |
S303 |
12 | BAA04g13250 | A04 | 18717088 | C | T | missense_variant | MODERATE | c.2138C>T|p.Ser713Phe |
S130 |
13 | BAA04g13250 | A04 | 18721866 | G | A | downstream_gene_variant | MODIFIER | c.*4582G>A| |
S195 |