Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05780 | A10 | 2963950 | C | T | missense_variant | MODERATE | c.460G>A|p.Asp154Asn |
S23 |
2 | BAA10g05780 | A10 | 2963958 | G | A | missense_variant | MODERATE | c.452C>T|p.Thr151Ile |
S167 |
3 | BAA10g05780 | A10 | 2964003 | G | A | missense_variant | MODERATE | c.407C>T|p.Ala136Val |
S293 |
4 | BAA10g05780 | A10 | 2964092 | C | T | synonymous_variant | LOW | c.318G>A|p.Pro106Pro |
S305 |
5 | BAA10g05780 | A10 | 2964234 | G | A | missense_variant | MODERATE | c.176C>T|p.Thr59Ile |
S1 S90 |
6 | BAA10g05780 | A10 | 2964340 | C | T | missense_variant | MODERATE | c.70G>A|p.Glu24Lys |
S44 |
7 | BAA10g05780 | A10 | 2965346 | C | T | upstream_gene_variant | MODIFIER | c.-937G>A| |
S174 S175 S27 |
8 | BAA10g05780 | A10 | 2965730 | G | A | upstream_gene_variant | MODIFIER | c.-1321C>T| |
S82 S92 |
9 | BAA10g05780 | A10 | 2965988 | C | T | upstream_gene_variant | MODIFIER | c.-1579G>A| |
S202 |
10 | BAA10g05780 | A10 | 2966425 | C | T | upstream_gene_variant | MODIFIER | c.-2016G>A| |
S42 |
11 | BAA10g05780 | A10 | 2967018 | C | T | upstream_gene_variant | MODIFIER | c.-2609G>A| |
S281 |
12 | BAA10g05780 | A10 | 2967272 | G | A | upstream_gene_variant | MODIFIER | c.-2863C>T| |
S115 |
13 | BAA10g05780 | A10 | 2968015 | C | T | upstream_gene_variant | MODIFIER | c.-3606G>A| |
S170 |
14 | BAA10g05780 | A10 | 2968029 | G | A | upstream_gene_variant | MODIFIER | c.-3620C>T| |
S277 |