Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g23780 | A10 | 19867921 | C | T | missense_variant | MODERATE | c.2965G>A|p.Val989Ile |
S281 |
2 | BAA10g23780 | A10 | 19868090 | C | T | splice_region_variant&synonymous_variant | LOW | c.2937G>A|p.Leu979Leu |
S282 |
3 | BAA10g23780 | A10 | 19869320 | G | A | missense_variant | MODERATE | c.2014C>T|p.Pro672Ser |
S59 |
4 | BAA10g23780 | A10 | 19869407 | C | T | missense_variant | MODERATE | c.1927G>A|p.Gly643Ser |
S292 |
5 | BAA10g23780 | A10 | 19870109 | C | T | missense_variant | MODERATE | c.1574G>A|p.Gly525Glu |
S48 |
6 | BAA10g23780 | A10 | 19870363 | C | T | synonymous_variant | LOW | c.1476G>A|p.Glu492Glu |
S210 |
7 | BAA10g23780 | A10 | 19870894 | C | T | synonymous_variant | LOW | c.1026G>A|p.Glu342Glu |
S206 S26 |
8 | BAA10g23780 | A10 | 19872373 | G | A | synonymous_variant | LOW | c.363C>T|p.Leu121Leu |
S207 |
9 | BAA10g23780 | A10 | 19872581 | G | A | missense_variant | MODERATE | c.155C>T|p.Ala52Val |
S66 |
10 | BAA10g23780 | A10 | 19872914 | C | T | upstream_gene_variant | MODIFIER | c.-23G>A| |
S292 |
11 | BAA10g23780 | A10 | 19873627 | C | T | upstream_gene_variant | MODIFIER | c.-736G>A| |
S54 |
12 | BAA10g23780 | A10 | 19873730 | A | G | upstream_gene_variant | MODIFIER | c.-839T>C| |
S302 |
13 | BAA10g23780 | A10 | 19875399 | C | T | upstream_gene_variant | MODIFIER | c.-2508G>A| |
S45 |
14 | BAA10g23780 | A10 | 19877778 | C | T | upstream_gene_variant | MODIFIER | c.-4887G>A| |
S185 |