Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g16830 | A10 | 16468482 | G | C | downstream_gene_variant | MODIFIER | c.*1996C>G| |
S268 |
2 | BAA10g16830 | A10 | 16469577 | G | A | downstream_gene_variant | MODIFIER | c.*901C>T| |
S172 S217 |
3 | BAA10g16830 | A10 | 16469799 | C | T | downstream_gene_variant | MODIFIER | c.*679G>A| |
S34 |
4 | BAA10g16830 | A10 | 16471036 | C | T | synonymous_variant | LOW | c.1875G>A|p.Thr625Thr |
S251 |
5 | BAA10g16830 | A10 | 16471041 | C | T | missense_variant | MODERATE | c.1870G>A|p.Ala624Thr |
S203 |
6 | BAA10g16830 | A10 | 16471215 | C | T | missense_variant | MODERATE | c.1696G>A|p.Glu566Lys |
S168 |
7 | BAA10g16830 | A10 | 16471506 | C | T | missense_variant | MODERATE | c.1405G>A|p.Val469Ile |
S115 |
8 | BAA10g16830 | A10 | 16472327 | C | T | missense_variant | MODERATE | c.584G>A|p.Arg195His |
S70 |
9 | BAA10g16830 | A10 | 16472487 | C | T | missense_variant | MODERATE | c.424G>A|p.Glu142Lys |
S281 |
10 | BAA10g16830 | A10 | 16472542 | G | A | synonymous_variant | LOW | c.369C>T|p.Ile123Ile |
S192 |
11 | BAA10g16830 | A10 | 16472670 | G | A | missense_variant | MODERATE | c.241C>T|p.Pro81Ser |
S184 |
12 | BAA10g16830 | A10 | 16472903 | C | T | missense_variant | MODERATE | c.8G>A|p.Arg3Lys |
S188 |
13 | BAA10g16830 | A10 | 16473465 | C | T | upstream_gene_variant | MODIFIER | c.-555G>A| |
S281 |
14 | BAA10g16830 | A10 | 16474003 | G | A | upstream_gene_variant | MODIFIER | c.-1093C>T| |
S163 |
15 | BAA10g16830 | A10 | 16476649 | C | T | upstream_gene_variant | MODIFIER | c.-3739G>A| |
S84 S93 |