Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01990 | A10 | 954294 | G | A | downstream_gene_variant | MODIFIER | c.*119C>T| |
S97 |
2 | BAA10g01990 | A10 | 954495 | G | A | intron_variant | MODIFIER | c.3386-72C>T| |
S13 |
3 | BAA10g01990 | A10 | 954574 | G | A | intron_variant | MODIFIER | c.3386-151C>T| |
S69 |
4 | BAA10g01990 | A10 | 954998 | G | A | intron_variant | MODIFIER | c.3385+447C>T| |
S76 |
5 | BAA10g01990 | A10 | 955143 | G | A | intron_variant | MODIFIER | c.3385+302C>T| |
S293 |
6 | BAA10g01990 | A10 | 956645 | C | T | missense_variant | MODERATE | c.2248G>A|p.Glu750Lys |
S287 |
7 | BAA10g01990 | A10 | 956691 | C | T | synonymous_variant | LOW | c.2202G>A|p.Lys734Lys |
S139 |
8 | BAA10g01990 | A10 | 957061 | C | T | missense_variant | MODERATE | c.1832G>A|p.Ser611Asn |
S197 |
9 | BAA10g01990 | A10 | 958003 | C | T | missense_variant | MODERATE | c.890G>A|p.Arg297Lys |
S114 |
10 | BAA10g01990 | A10 | 959782 | G | A | upstream_gene_variant | MODIFIER | c.-477C>T| |
S219 S72 |
11 | BAA10g01990 | A10 | 960436 | G | A | upstream_gene_variant | MODIFIER | c.-1131C>T| |
S215 |
12 | BAA10g01990 | A10 | 960768 | C | T | upstream_gene_variant | MODIFIER | c.-1463G>A| |
S149 |
13 | BAA10g01990 | A10 | 961130 | C | T | upstream_gene_variant | MODIFIER | c.-1825G>A| |
S171 |
14 | BAA10g01990 | A10 | 962361 | C | T | upstream_gene_variant | MODIFIER | c.-3056G>A| |
S294 |
15 | BAA10g01990 | A10 | 964274 | C | T | upstream_gene_variant | MODIFIER | c.-4969G>A| |
S204 |