Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g21390 | A08 | 16221924 | C | T | synonymous_variant | LOW | c.5574G>A|p.Val1858Val |
S178 |
2 | BAA08g21390 | A08 | 16222219 | C | T | missense_variant | MODERATE | c.5279G>A|p.Gly1760Glu |
S190 S211 S227 |
3 | BAA08g21390 | A08 | 16222796 | C | T | missense_variant | MODERATE | c.4702G>A|p.Ala1568Thr |
S271 |
4 | BAA08g21390 | A08 | 16222956 | G | A | synonymous_variant | LOW | c.4542C>T|p.His1514His |
S62 |
5 | BAA08g21390 | A08 | 16223261 | G | A | missense_variant | MODERATE | c.4237C>T|p.Pro1413Ser |
S5 |
6 | BAA08g21390 | A08 | 16223314 | G | A | missense_variant | MODERATE | c.4184C>T|p.Ser1395Phe |
S40 S49 |
7 | BAA08g21390 | A08 | 16223560 | G | A | missense_variant | MODERATE | c.4007C>T|p.Ser1336Phe |
S289 S290 |
8 | BAA08g21390 | A08 | 16223812 | G | A | synonymous_variant | LOW | c.3837C>T|p.Val1279Val |
S32 |
9 | BAA08g21390 | A08 | 16224775 | C | T | missense_variant | MODERATE | c.3088G>A|p.Glu1030Lys |
S139 |
10 | BAA08g21390 | A08 | 16225480 | C | T | missense_variant | MODERATE | c.2383G>A|p.Glu795Lys |
S181 |
11 | BAA08g21390 | A08 | 16225902 | G | A | missense_variant | MODERATE | c.2038C>T|p.Pro680Ser |
S37 |
12 | BAA08g21390 | A08 | 16226831 | G | A | missense_variant | MODERATE | c.1180C>T|p.Pro394Ser |
S162 |
13 | BAA08g21390 | A08 | 16227133 | C | T | missense_variant | MODERATE | c.878G>A|p.Gly293Asp |
S19 |
14 | BAA08g21390 | A08 | 16229704 | G | A | upstream_gene_variant | MODIFIER | c.-1459C>T| |
S133 |
15 | BAA08g21390 | A08 | 16229778 | C | T | upstream_gene_variant | MODIFIER | c.-1533G>A| |
S271 |