Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19080 | A10 | 17634527 | T | A | missense_variant | MODERATE | c.1324A>T|p.Ser442Cys |
S33 |
2 | BAA10g19080 | A10 | 17636125 | C | T | missense_variant | MODERATE | c.939G>A|p.Met313Ile |
S144 |
3 | BAA10g19080 | A10 | 17636982 | C | T | missense_variant | MODERATE | c.583G>A|p.Glu195Lys |
S297 |
4 | BAA10g19080 | A10 | 17637025 | C | T | missense_variant | MODERATE | c.540G>A|p.Met180Ile |
S92 |
5 | BAA10g19080 | A10 | 17638546 | C | T | missense_variant | MODERATE | c.187G>A|p.Glu63Lys |
S296 |
6 | BAA10g19080 | A10 | 17639278 | G | A | upstream_gene_variant | MODIFIER | c.-329C>T| |
S163 |
7 | BAA10g19080 | A10 | 17639476 | C | T | upstream_gene_variant | MODIFIER | c.-527G>A| |
S123 |
8 | BAA10g19080 | A10 | 17640036 | G | A | upstream_gene_variant | MODIFIER | c.-1087C>T| |
S132 S137 S215 S89 |
9 | BAA10g19080 | A10 | 17640091 | C | T | upstream_gene_variant | MODIFIER | c.-1142G>A| |
S262 |
10 | BAA10g19080 | A10 | 17641372 | C | T | upstream_gene_variant | MODIFIER | c.-2423G>A| |
S251 |
11 | BAA10g19080 | A10 | 17641565 | C | T | upstream_gene_variant | MODIFIER | c.-2616G>A| |
S185 |
12 | BAA10g19080 | A10 | 17641701 | G | A | upstream_gene_variant | MODIFIER | c.-2752C>T| |
S136 |
13 | BAA10g19080 | A10 | 17641764 | C | T | upstream_gene_variant | MODIFIER | c.-2815G>A| |
S276 |
14 | BAA10g19080 | A10 | 17643442 | G | A | upstream_gene_variant | MODIFIER | c.-4493C>T| |
S127 |
15 | BAA10g19080 | A10 | 17643479 | G | A | upstream_gene_variant | MODIFIER | c.-4530C>T| |
S138 |
16 | BAA10g19080 | A10 | 17643918 | C | T | upstream_gene_variant | MODIFIER | c.-4969G>A| |
S281 |