Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g27800 | A08 | 19484143 | C | T | upstream_gene_variant | MODIFIER | c.-2324C>T| |
S219 S72 |
2 | BAA08g27800 | A08 | 19484168 | C | T | upstream_gene_variant | MODIFIER | c.-2299C>T| |
S113 |
3 | BAA08g27800 | A08 | 19485164 | G | A | upstream_gene_variant | MODIFIER | c.-1303G>A| |
S125 |
4 | BAA08g27800 | A08 | 19486016 | C | T | upstream_gene_variant | MODIFIER | c.-451C>T| |
S134 |
5 | BAA08g27800 | A08 | 19486122 | C | T | upstream_gene_variant | MODIFIER | c.-345C>T| |
S230 |
6 | BAA08g27800 | A08 | 19486848 | G | A | missense_variant | MODERATE | c.382G>A|p.Glu128Lys |
S219 S72 |
7 | BAA08g27800 | A08 | 19487355 | T | G | missense_variant | MODERATE | c.889T>G|p.Cys297Gly |
S130 S166 S192 S251 S277 S278 S36 S52 S75 S85 |
8 | BAA08g27800 | A08 | 19487936 | G | A | synonymous_variant | LOW | c.1470G>A|p.Lys490Lys |
S188 |
9 | BAA08g27800 | A08 | 19488930 | G | A | missense_variant | MODERATE | c.2464G>A|p.Asp822Asn |
S116 |
10 | BAA08g27800 | A08 | 19489297 | G | A | missense_variant | MODERATE | c.2831G>A|p.Gly944Asp |
S142 |
11 | BAA08g27800 | A08 | 19489491 | G | A | missense_variant | MODERATE | c.3025G>A|p.Asp1009Asn |
S182 |
12 | BAA08g27800 | A08 | 19489576 | C | T | missense_variant | MODERATE | c.3110C>T|p.Ser1037Leu |
S41 |
13 | BAA08g27800 | A08 | 19489580 | G | A | synonymous_variant | LOW | c.3114G>A|p.Ser1038Ser |
S151 S263 S279 |
14 | BAA08g27800 | A08 | 19490835 | C | T | missense_variant | MODERATE | c.3962C>T|p.Ser1321Phe |
S47 |
15 | BAA08g27800 | A08 | 19491960 | C | T | synonymous_variant | LOW | c.4563C>T|p.Asp1521Asp |
S74 |