Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g40260 | A06 | 26177201 | G | A | synonymous_variant | LOW | c.1806C>T|p.Pro602Pro |
S119 S267 |
2 | BAA06g40260 | A06 | 26177895 | C | T | missense_variant | MODERATE | c.1375G>A|p.Glu459Lys |
S15 S3 |
3 | BAA06g40260 | A06 | 26181019 | G | A | intron_variant | MODIFIER | c.900+200C>T| |
S47 |
4 | BAA06g40260 | A06 | 26181896 | C | T | intron_variant | MODIFIER | c.666-443G>A| |
S68 |
5 | BAA06g40260 | A06 | 26182505 | G | A | intron_variant | MODIFIER | c.666-1052C>T| |
S156 |
6 | BAA06g40260 | A06 | 26185053 | T | A | intron_variant | MODIFIER | c.666-3600A>T| |
S206 |
7 | BAA06g40260 | A06 | 26186347 | C | T | intron_variant | MODIFIER | c.666-4894G>A| |
S43 |
8 | BAA06g40260 | A06 | 26186563 | C | T | intron_variant | MODIFIER | c.666-5110G>A| |
S115 |
9 | BAA06g40260 | A06 | 26188709 | C | T | intron_variant | MODIFIER | c.665+3298G>A| |
S242 |
10 | BAA06g40260 | A06 | 26189989 | G | A | intron_variant | MODIFIER | c.665+2018C>T| |
S206 S26 |
11 | BAA06g40260 | A06 | 26190490 | C | T | intron_variant | MODIFIER | c.665+1517G>A| |
S280 |
12 | BAA06g40260 | A06 | 26191194 | C | T | intron_variant | MODIFIER | c.665+813G>A| |
S148 S30 S31 |
13 | BAA06g40260 | A06 | 26192050 | C | T | missense_variant | MODERATE | c.622G>A|p.Val208Ile |
S295 |
14 | BAA06g40260 | A06 | 26198440 | C | T | upstream_gene_variant | MODIFIER | c.-3685G>A| |
S135 |
15 | BAA06g40260 | A06 | 26198455 | C | T | upstream_gene_variant | MODIFIER | c.-3700G>A| |
S187 |