Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07970 | A10 | 5041530 | C | T | downstream_gene_variant | MODIFIER | c.*1791G>A| |
S282 |
2 | BAA10g07970 | A10 | 5043443 | C | T | missense_variant | MODERATE | c.2188G>A|p.Gly730Ser |
S19 |
3 | BAA10g07970 | A10 | 5043597 | C | T | synonymous_variant | LOW | c.2034G>A|p.Gly678Gly |
S301 S304 |
4 | BAA10g07970 | A10 | 5044942 | G | A | splice_region_variant&intron_variant | LOW | c.1200+5C>T| |
S198 |
5 | BAA10g07970 | A10 | 5044976 | G | A | missense_variant | MODERATE | c.1171C>T|p.Leu391Phe |
S20 |
6 | BAA10g07970 | A10 | 5045164 | C | T | missense_variant | MODERATE | c.1084G>A|p.Val362Ile |
S150 |
7 | BAA10g07970 | A10 | 5046322 | G | A | synonymous_variant | LOW | c.240C>T|p.Phe80Phe |
S207 |
8 | BAA10g07970 | A10 | 5046565 | C | T | upstream_gene_variant | MODIFIER | c.-4G>A| |
S135 |
9 | BAA10g07970 | A10 | 5048046 | G | A | upstream_gene_variant | MODIFIER | c.-1485C>T| |
S43 |
10 | BAA10g07970 | A10 | 5048163 | C | T | upstream_gene_variant | MODIFIER | c.-1602G>A| |
S132 S137 S215 |
11 | BAA10g07970 | A10 | 5049050 | G | A | upstream_gene_variant | MODIFIER | c.-2489C>T| |
S293 |
12 | BAA10g07970 | A10 | 5049128 | C | T | upstream_gene_variant | MODIFIER | c.-2567G>A| |
S88 |
13 | BAA10g07970 | A10 | 5049597 | G | A | upstream_gene_variant | MODIFIER | c.-3036C>T| |
S296 |
14 | BAA10g07970 | A10 | 5049938 | C | T | upstream_gene_variant | MODIFIER | c.-3377G>A| |
S113 |
15 | BAA10g07970 | A10 | 5050443 | G | A | upstream_gene_variant | MODIFIER | c.-3882C>T| |
S45 |
16 | BAA10g07970 | A10 | 5050833 | G | A | upstream_gene_variant | MODIFIER | c.-4272C>T| |
S265 |
17 | BAA10g07970 | A10 | 5051463 | C | T | upstream_gene_variant | MODIFIER | c.-4902G>A| |
S276 |