Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g19480 | A04 | 22970320 | G | A | downstream_gene_variant | MODIFIER | c.*4244C>T| |
S165 |
2 | BAA04g19480 | A04 | 22971691 | C | T | downstream_gene_variant | MODIFIER | c.*2873G>A| |
S244 |
3 | BAA04g19480 | A04 | 22973338 | C | T | downstream_gene_variant | MODIFIER | c.*1226G>A| |
S284 |
4 | BAA04g19480 | A04 | 22973729 | C | T | downstream_gene_variant | MODIFIER | c.*835G>A| |
S163 |
5 | BAA04g19480 | A04 | 22974658 | G | A | missense_variant | MODERATE | c.2054C>T|p.Ala685Val |
S280 |
6 | BAA04g19480 | A04 | 22974900 | C | T | synonymous_variant | LOW | c.1812G>A|p.Glu604Glu |
S292 |
7 | BAA04g19480 | A04 | 22975007 | G | A | stop_gained | HIGH | c.1705C>T|p.Arg569* |
S11 |
8 | BAA04g19480 | A04 | 22975109 | C | T | missense_variant | MODERATE | c.1603G>A|p.Asp535Asn |
S144 |
9 | BAA04g19480 | A04 | 22975326 | C | T | missense_variant | MODERATE | c.1386G>A|p.Met462Ile |
S242 |
10 | BAA04g19480 | A04 | 22975737 | C | T | missense_variant | MODERATE | c.1073G>A|p.Gly358Glu |
S130 |
11 | BAA04g19480 | A04 | 22977044 | G | A | missense_variant | MODERATE | c.82C>T|p.Leu28Phe |
S223 |
12 | BAA04g19480 | A04 | 22977825 | G | A | upstream_gene_variant | MODIFIER | c.-492C>T| |
S72 S78 |
13 | BAA04g19480 | A04 | 22977827 | C | T | upstream_gene_variant | MODIFIER | c.-494G>A| |
S84 S93 |
14 | BAA04g19480 | A04 | 22978469 | C | T | upstream_gene_variant | MODIFIER | c.-1136G>A| |
S178 |
15 | BAA04g19480 | A04 | 22979305 | G | A | upstream_gene_variant | MODIFIER | c.-1972C>T| |
S15 S3 |
16 | BAA04g19480 | A04 | 22981378 | G | A | upstream_gene_variant | MODIFIER | c.-4045C>T| |
S120 |
17 | BAA04g19480 | A04 | 22982326 | G | A | upstream_gene_variant | MODIFIER | c.-4993C>T| |
S52 |