Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g07340 | A07 | 16570925 | G | A | upstream_gene_variant | MODIFIER | c.-4942G>A| |
S186 |
2 | BAA07g07340 | A07 | 16572047 | C | T | upstream_gene_variant | MODIFIER | c.-3820C>T| |
S68 |
3 | BAA07g07340 | A07 | 16572596 | G | A | upstream_gene_variant | MODIFIER | c.-3271G>A| |
S107 |
4 | BAA07g07340 | A07 | 16573909 | C | T | upstream_gene_variant | MODIFIER | c.-1958C>T| |
S266 |
5 | BAA07g07340 | A07 | 16575008 | C | T | upstream_gene_variant | MODIFIER | c.-859C>T| |
S261 |
6 | BAA07g07340 | A07 | 16575665 | G | A | upstream_gene_variant | MODIFIER | c.-202G>A| |
S176 |
7 | BAA07g07340 | A07 | 16575900 | G | A | missense_variant | MODERATE | c.34G>A|p.Asp12Asn |
S291 |
8 | BAA07g07340 | A07 | 16576361 | G | A | intron_variant | MODIFIER | c.282-30G>A| |
S110 |
9 | BAA07g07340 | A07 | 16576935 | G | A | missense_variant | MODERATE | c.826G>A|p.Glu276Lys |
S92 |
10 | BAA07g07340 | A07 | 16577066 | G | A | synonymous_variant | LOW | c.957G>A|p.Gln319Gln |
S183 |
11 | BAA07g07340 | A07 | 16577134 | G | A | missense_variant | MODERATE | c.1025G>A|p.Gly342Glu |
S283 |
12 | BAA07g07340 | A07 | 16577572 | G | A | missense_variant | MODERATE | c.1463G>A|p.Gly488Glu |
S5 |
13 | BAA07g07340 | A07 | 16577840 | C | T | missense_variant&splice_region_variant | MODERATE | c.1631C>T|p.Ala544Val |
S162 |
14 | BAA07g07340 | A07 | 16578265 | G | A | synonymous_variant | LOW | c.1845G>A|p.Lys615Lys |
S264 |
15 | BAA07g07340 | A07 | 16578616 | C | T | intron_variant | MODIFIER | c.1948-87C>T| |
S224 |
16 | BAA07g07340 | A07 | 16579233 | C | T | splice_region_variant&intron_variant | LOW | c.2275+8C>T| |
S162 |
17 | BAA07g07340 | A07 | 16579238 | C | T | intron_variant | MODIFIER | c.2275+13C>T| |
|
18 | BAA07g07340 | A07 | 16579438 | C | T | missense_variant | MODERATE | c.2416C>T|p.Arg806Trp |
S152 |
19 | BAA07g07340 | A07 | 16580147 | G | A | intron_variant | MODIFIER | c.2821-28G>A| |
S228 |
20 | BAA07g07340 | A07 | 16580329 | G | A | intron_variant | MODIFIER | c.2866+109G>A| |
S268 |
21 | BAA07g07340 | A07 | 16580856 | C | T | missense_variant | MODERATE | c.3083C>T|p.Ser1028Phe |
S167 |
22 | BAA07g07340 | A07 | 16582193 | G | A | splice_region_variant&intron_variant | LOW | c.3551+5G>A| |
S131 |
23 | BAA07g07340 | A07 | 16582634 | G | A | missense_variant | MODERATE | c.3799G>A|p.Asp1267Asn |
S269 |
24 | BAA07g07340 | A07 | 16583181 | C | T | missense_variant | MODERATE | c.4244C>T|p.Ser1415Phe |
S85 |
25 | BAA07g07340 | A07 | 16583550 | C | T | missense_variant | MODERATE | c.4613C>T|p.Ala1538Val |
S63 |