Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g27760 | A08 | 19462728 | G | A | synonymous_variant | LOW | c.69G>A|p.Lys23Lys |
S64 |
2 | BAA08g27760 | A08 | 19465308 | C | T | missense_variant | MODERATE | c.1225C>T|p.Leu409Phe |
S169 |
3 | BAA08g27760 | A08 | 19466568 | C | T | synonymous_variant | LOW | c.1740C>T|p.Leu580Leu |
S280 |
4 | BAA08g27760 | A08 | 19466769 | G | A | missense_variant | MODERATE | c.1819G>A|p.Val607Met |
S91 |
5 | BAA08g27760 | A08 | 19466943 | G | A | missense_variant | MODERATE | c.1883G>A|p.Ser628Asn |
S195 S251 |
6 | BAA08g27760 | A08 | 19466965 | G | A | synonymous_variant | LOW | c.1905G>A|p.Arg635Arg |
S238 |
7 | BAA08g27760 | A08 | 19467112 | C | T | synonymous_variant | LOW | c.2052C>T|p.Asp684Asp |
S278 |
8 | BAA08g27760 | A08 | 19468107 | G | A | intron_variant | MODIFIER | c.2409+79G>A| |
S286 |
9 | BAA08g27760 | A08 | 19469212 | C | T | missense_variant | MODERATE | c.2882C>T|p.Ala961Val |
S205 |
10 | BAA08g27760 | A08 | 19469604 | C | T | missense_variant | MODERATE | c.3113C>T|p.Ser1038Leu |
S89 |
11 | BAA08g27760 | A08 | 19471395 | C | T | downstream_gene_variant | MODIFIER | c.*1736C>T| |
S208 |
12 | BAA08g27760 | A08 | 19471493 | G | A | downstream_gene_variant | MODIFIER | c.*1834G>A| |
S257 |
13 | BAA08g27760 | A08 | 19473072 | C | T | downstream_gene_variant | MODIFIER | c.*3413C>T| |
S205 S209 |
14 | BAA08g27760 | A08 | 19474479 | G | A | downstream_gene_variant | MODIFIER | c.*4820G>A| |
S190 |