Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01940 | A08 | 1451111 | C | T | upstream_gene_variant | MODIFIER | c.-4195C>T| |
S14 |
2 | BAA08g01940 | A08 | 1452183 | G | A | upstream_gene_variant | MODIFIER | c.-3123G>A| |
S234 |
3 | BAA08g01940 | A08 | 1452465 | C | T | upstream_gene_variant | MODIFIER | c.-2841C>T| |
S289 S290 |
4 | BAA08g01940 | A08 | 1452544 | G | A | upstream_gene_variant | MODIFIER | c.-2762G>A| |
S281 |
5 | BAA08g01940 | A08 | 1453384 | G | A | upstream_gene_variant | MODIFIER | c.-1922G>A| |
S221 |
6 | BAA08g01940 | A08 | 1453452 | G | A | upstream_gene_variant | MODIFIER | c.-1854G>A| |
S279 |
7 | BAA08g01940 | A08 | 1454724 | C | T | upstream_gene_variant | MODIFIER | c.-582C>T| |
S292 |
8 | BAA08g01940 | A08 | 1455124 | G | A | upstream_gene_variant | MODIFIER | c.-182G>A| |
S68 |
9 | BAA08g01940 | A08 | 1455358 | G | A | missense_variant | MODERATE | c.53G>A|p.Gly18Glu |
S121 |
10 | BAA08g01940 | A08 | 1455525 | C | T | missense_variant | MODERATE | c.220C>T|p.Pro74Ser |
S201 |
11 | BAA08g01940 | A08 | 1455714 | T | A | missense_variant | MODERATE | c.291T>A|p.Asn97Lys |
S290 |
12 | BAA08g01940 | A08 | 1455773 | C | T | missense_variant | MODERATE | c.350C>T|p.Ser117Phe |
S114 |
13 | BAA08g01940 | A08 | 1455833 | G | A | splice_region_variant&intron_variant | LOW | c.403+7G>A| |
S301 S304 |
14 | BAA08g01940 | A08 | 1455918 | G | A | missense_variant | MODERATE | c.421G>A|p.Asp141Asn |
S19 |