Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g33150 | A10 | 23660266 | C | T | missense_variant | MODERATE | c.3379G>A|p.Val1127Ile |
S152 |
2 | BAA10g33150 | A10 | 23660421 | C | T | missense_variant | MODERATE | c.3224G>A|p.Arg1075Lys |
S234 |
3 | BAA10g33150 | A10 | 23661012 | C | T | missense_variant | MODERATE | c.2633G>A|p.Arg878Lys |
S287 |
4 | BAA10g33150 | A10 | 23661218 | C | T | synonymous_variant | LOW | c.2427G>A|p.Ser809Ser |
S200 |
5 | BAA10g33150 | A10 | 23661793 | C | T | missense_variant | MODERATE | c.1931G>A|p.Arg644Lys |
S266 |
6 | BAA10g33150 | A10 | 23661893 | C | T | missense_variant | MODERATE | c.1831G>A|p.Glu611Lys |
S234 |
7 | BAA10g33150 | A10 | 23662215 | C | T | missense_variant | MODERATE | c.1585G>A|p.Glu529Lys |
S262 |
8 | BAA10g33150 | A10 | 23663720 | C | T | missense_variant | MODERATE | c.740G>A|p.Ser247Asn |
S292 |
9 | BAA10g33150 | A10 | 23663775 | C | T | missense_variant | MODERATE | c.685G>A|p.Asp229Asn |
S123 |
10 | BAA10g33150 | A10 | 23664421 | C | T | synonymous_variant | LOW | c.39G>A|p.Lys13Lys |
S282 |
11 | BAA10g33150 | A10 | 23664514 | C | T | upstream_gene_variant | MODIFIER | c.-55G>A| |
S282 |
12 | BAA10g33150 | A10 | 23666869 | G | A | upstream_gene_variant | MODIFIER | c.-2410C>T| |
S173 |
13 | BAA10g33150 | A10 | 23668718 | G | A | upstream_gene_variant | MODIFIER | c.-4259C>T| |
S274 |