Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g11470 | A09 | 6440857 | C | T | downstream_gene_variant | MODIFIER | c.*1268G>A| |
S28 |
2 | BAA09g11470 | A09 | 6443223 | G | A | missense_variant | MODERATE | c.1273C>T|p.Arg425Cys |
S25 |
3 | BAA09g11470 | A09 | 6443296 | G | A | synonymous_variant | LOW | c.1200C>T|p.Leu400Leu |
S25 |
4 | BAA09g11470 | A09 | 6443905 | C | T | missense_variant | MODERATE | c.899G>A|p.Gly300Asp |
S250 |
5 | BAA09g11470 | A09 | 6443944 | C | T | missense_variant | MODERATE | c.860G>A|p.Ser287Asn |
S36 |
6 | BAA09g11470 | A09 | 6444139 | C | T | missense_variant | MODERATE | c.665G>A|p.Arg222Gln |
S123 |
7 | BAA09g11470 | A09 | 6444255 | C | T | synonymous_variant | LOW | c.549G>A|p.Gln183Gln |
S19 |
8 | BAA09g11470 | A09 | 6444261 | G | A | synonymous_variant | LOW | c.543C>T|p.Asn181Asn |
S32 |
9 | BAA09g11470 | A09 | 6444383 | G | A | missense_variant | MODERATE | c.421C>T|p.Leu141Phe |
S82 S92 |
10 | BAA09g11470 | A09 | 6444967 | G | A | upstream_gene_variant | MODIFIER | c.-79C>T| |
S236 |
11 | BAA09g11470 | A09 | 6447880 | C | T | upstream_gene_variant | MODIFIER | c.-2992G>A| |
S138 |
12 | BAA09g11470 | A09 | 6447953 | G | A | upstream_gene_variant | MODIFIER | c.-3065C>T| |
S181 |
13 | BAA09g11470 | A09 | 6448615 | G | A | upstream_gene_variant | MODIFIER | c.-3727C>T| |
S240 |
14 | BAA09g11470 | A09 | 6448653 | C | T | upstream_gene_variant | MODIFIER | c.-3765G>A| |
S43 |
15 | BAA09g11470 | A09 | 6449884 | C | T | upstream_gene_variant | MODIFIER | c.-4996G>A| |
S236 |