Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g45130 | A06 | 28801824 | G | A | synonymous_variant | LOW | c.2889C>T|p.Val963Val |
S283 |
2 | BAA06g45130 | A06 | 28802011 | C | T | missense_variant | MODERATE | c.2702G>A|p.Gly901Glu |
S293 |
3 | BAA06g45130 | A06 | 28802791 | C | T | missense_variant | MODERATE | c.2081G>A|p.Gly694Glu |
S179 |
4 | BAA06g45130 | A06 | 28802879 | G | A | missense_variant | MODERATE | c.1993C>T|p.Leu665Phe |
S76 |
5 | BAA06g45130 | A06 | 28804323 | G | A | missense_variant | MODERATE | c.965C>T|p.Ser322Phe |
S237 |
6 | BAA06g45130 | A06 | 28804409 | C | T | synonymous_variant | LOW | c.879G>A|p.Lys293Lys |
S288 |
7 | BAA06g45130 | A06 | 28804533 | G | A | missense_variant | MODERATE | c.755C>T|p.Ser252Leu |
S122 |
8 | BAA06g45130 | A06 | 28804589 | G | A | synonymous_variant | LOW | c.699C>T|p.Phe233Phe |
S216 |
9 | BAA06g45130 | A06 | 28804966 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.431-1G>A| |
S286 |
10 | BAA06g45130 | A06 | 28805080 | G | A | missense_variant | MODERATE | c.397C>T|p.Pro133Ser |
S293 |
11 | BAA06g45130 | A06 | 28805242 | G | A | missense_variant | MODERATE | c.332C>T|p.Ser111Phe |
S295 |
12 | BAA06g45130 | A06 | 28805609 | G | A | splice_region_variant&intron_variant | LOW | c.37-3C>T| |
S135 |
13 | BAA06g45130 | A06 | 28807213 | G | A | upstream_gene_variant | MODIFIER | c.-1483C>T| |
S163 |
14 | BAA06g45130 | A06 | 28807481 | G | A | upstream_gene_variant | MODIFIER | c.-1751C>T| |
S60 |
15 | BAA06g45130 | A06 | 28808355 | G | A | upstream_gene_variant | MODIFIER | c.-2625C>T| |
S28 |
16 | BAA06g45130 | A06 | 28808616 | C | T | upstream_gene_variant | MODIFIER | c.-2886G>A| |
S278 |
17 | BAA06g45130 | A06 | 28809137 | C | T | upstream_gene_variant | MODIFIER | c.-3407G>A| |
S72 |