Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g01840 | A04 | 1063876 | G | A | intron_variant | MODIFIER | c.2611-27C>T| |
S12 |
2 | BAA04g01840 | A04 | 1064347 | G | A | intron_variant | MODIFIER | c.2427+87C>T| |
S41 |
3 | BAA04g01840 | A04 | 1065516 | G | A | intron_variant | MODIFIER | c.1700-42C>T| |
S216 |
4 | BAA04g01840 | A04 | 1066306 | G | A | missense_variant | MODERATE | c.1406C>T|p.Pro469Leu |
S279 |
5 | BAA04g01840 | A04 | 1066683 | G | A | synonymous_variant | LOW | c.1194C>T|p.Leu398Leu |
S78 |
6 | BAA04g01840 | A04 | 1066767 | C | T | splice_region_variant&intron_variant | LOW | c.1170+6G>A| |
S265 |
7 | BAA04g01840 | A04 | 1067032 | C | T | missense_variant | MODERATE | c.979G>A|p.Asp327Asn |
S48 |
8 | BAA04g01840 | A04 | 1067047 | C | T | missense_variant | MODERATE | c.964G>A|p.Glu322Lys |
S110 |
9 | BAA04g01840 | A04 | 1069393 | C | T | upstream_gene_variant | MODIFIER | c.-641G>A| |
S92 |
10 | BAA04g01840 | A04 | 1069440 | G | A | upstream_gene_variant | MODIFIER | c.-688C>T| |
S136 |
11 | BAA04g01840 | A04 | 1069558 | C | T | upstream_gene_variant | MODIFIER | c.-806G>A| |
S107 |
12 | BAA04g01840 | A04 | 1071061 | C | T | upstream_gene_variant | MODIFIER | c.-2309G>A| |
S173 |
13 | BAA04g01840 | A04 | 1071103 | G | A | upstream_gene_variant | MODIFIER | c.-2351C>T| |
S263 |
14 | BAA04g01840 | A04 | 1071686 | C | T | upstream_gene_variant | MODIFIER | c.-2934G>A| |
S1 S10 S90 |
15 | BAA04g01840 | A04 | 1072248 | G | A | upstream_gene_variant | MODIFIER | c.-3496C>T| |
S199 |