Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g33680 | A10 | 23912566 | C | T | downstream_gene_variant | MODIFIER | c.*1516G>A| |
S2 |
2 | BAA10g33680 | A10 | 23912575 | G | A | downstream_gene_variant | MODIFIER | c.*1507C>T| |
S289 S290 |
3 | BAA10g33680 | A10 | 23912964 | C | T | downstream_gene_variant | MODIFIER | c.*1118G>A| |
S305 |
4 | BAA10g33680 | A10 | 23914160 | G | A | synonymous_variant | LOW | c.2436C>T|p.Tyr812Tyr |
S299 |
5 | BAA10g33680 | A10 | 23914737 | C | T | missense_variant | MODERATE | c.2095G>A|p.Asp699Asn |
S5 |
6 | BAA10g33680 | A10 | 23915678 | G | A | missense_variant | MODERATE | c.1562C>T|p.Pro521Leu |
S179 |
7 | BAA10g33680 | A10 | 23915720 | G | A | missense_variant | MODERATE | c.1520C>T|p.Thr507Ile |
S94 |
8 | BAA10g33680 | A10 | 23916208 | G | A | splice_region_variant&synonymous_variant | LOW | c.1218C>T|p.Ser406Ser |
S32 |
9 | BAA10g33680 | A10 | 23919418 | C | T | splice_donor_variant&intron_variant | HIGH | c.136+1G>A| |
S225 S73 |
10 | BAA10g33680 | A10 | 23919833 | C | T | upstream_gene_variant | MODIFIER | c.-279G>A| |
S277 |
11 | BAA10g33680 | A10 | 23920473 | G | A | upstream_gene_variant | MODIFIER | c.-919C>T| |
S99 |
12 | BAA10g33680 | A10 | 23924096 | C | T | upstream_gene_variant | MODIFIER | c.-4542G>A| |
S37 |
13 | BAA10g33680 | A10 | 23924183 | C | T | upstream_gene_variant | MODIFIER | c.-4629G>A| |
S221 |
14 | BAA10g33680 | A10 | 23924266 | G | A | upstream_gene_variant | MODIFIER | c.-4712C>T| |
S173 |