Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08390 | A10 | 10132656 | G | A | downstream_gene_variant | MODIFIER | c.*775C>T| |
S226 |
2 | BAA10g08390 | A10 | 10133459 | G | A | missense_variant | MODERATE | c.2873C>T|p.Ser958Phe |
S69 |
3 | BAA10g08390 | A10 | 10133698 | C | T | stop_gained | HIGH | c.2634G>A|p.Trp878* |
S244 |
4 | BAA10g08390 | A10 | 10134148 | C | T | intron_variant | MODIFIER | c.2503+54G>A| |
S193 |
5 | BAA10g08390 | A10 | 10134542 | G | A | synonymous_variant | LOW | c.2163C>T|p.Ile721Ile |
S295 |
6 | BAA10g08390 | A10 | 10134644 | C | T | stop_gained | HIGH | c.2061G>A|p.Trp687* |
S203 |
7 | BAA10g08390 | A10 | 10134826 | C | T | missense_variant | MODERATE | c.1879G>A|p.Asp627Asn |
S206 S26 |
8 | BAA10g08390 | A10 | 10134932 | C | T | synonymous_variant | LOW | c.1773G>A|p.Leu591Leu |
S67 |
9 | BAA10g08390 | A10 | 10135306 | G | A | missense_variant | MODERATE | c.1399C>T|p.Leu467Phe |
S67 |
10 | BAA10g08390 | A10 | 10135316 | C | T | synonymous_variant | LOW | c.1389G>A|p.Val463Val |
S79 S91 |
11 | BAA10g08390 | A10 | 10135758 | C | T | missense_variant | MODERATE | c.947G>A|p.Arg316Lys |
S297 |
12 | BAA10g08390 | A10 | 10135891 | C | T | missense_variant | MODERATE | c.814G>A|p.Asp272Asn |
S131 |
13 | BAA10g08390 | A10 | 10137192 | G | A | upstream_gene_variant | MODIFIER | c.-488C>T| |
S221 |
14 | BAA10g08390 | A10 | 10137497 | C | A | upstream_gene_variant | MODIFIER | c.-793G>T| |
S146 |
15 | BAA10g08390 | A10 | 10137872 | G | A | upstream_gene_variant | MODIFIER | c.-1168C>T| |
S68 |
16 | BAA10g08390 | A10 | 10138035 | T | A | upstream_gene_variant | MODIFIER | c.-1331A>T| |
S108 |
17 | BAA10g08390 | A10 | 10139103 | G | A | upstream_gene_variant | MODIFIER | c.-2399C>T| |
S198 |
18 | BAA10g08390 | A10 | 10139521 | C | T | upstream_gene_variant | MODIFIER | c.-2817G>A| |
S155 S211 |
19 | BAA10g08390 | A10 | 10139809 | G | A | upstream_gene_variant | MODIFIER | c.-3105C>T| |
S13 |
20 | BAA10g08390 | A10 | 10141668 | C | T | upstream_gene_variant | MODIFIER | c.-4964G>A| |
S287 |