Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g13990 | A06 | 6907340 | C | T | upstream_gene_variant | MODIFIER | c.-3567C>T| |
S267 S90 |
2 | BAA06g13990 | A06 | 6908771 | C | T | upstream_gene_variant | MODIFIER | c.-2136C>T| |
S188 |
3 | BAA06g13990 | A06 | 6908828 | A | G | upstream_gene_variant | MODIFIER | c.-2079A>G| |
S292 |
4 | BAA06g13990 | A06 | 6910077 | G | A | upstream_gene_variant | MODIFIER | c.-830G>A| |
S72 |
5 | BAA06g13990 | A06 | 6911915 | G | A | missense_variant | MODERATE | c.545G>A|p.Arg182Lys |
S273 |
6 | BAA06g13990 | A06 | 6911923 | G | A | missense_variant | MODERATE | c.553G>A|p.Asp185Asn |
S169 |
7 | BAA06g13990 | A06 | 6913146 | G | A | missense_variant | MODERATE | c.1568G>A|p.Arg523His |
S221 |
8 | BAA06g13990 | A06 | 6914419 | G | A | synonymous_variant | LOW | c.2757G>A|p.Arg919Arg |
S292 |
9 | BAA06g13990 | A06 | 6914461 | G | A | synonymous_variant | LOW | c.2799G>A|p.Gly933Gly |
S86 |
10 | BAA06g13990 | A06 | 6914514 | C | T | missense_variant | MODERATE | c.2852C>T|p.Ser951Phe |
S296 |
11 | BAA06g13990 | A06 | 6915183 | G | A | downstream_gene_variant | MODIFIER | c.*401G>A| |
S81 S85 |
12 | BAA06g13990 | A06 | 6916469 | C | T | downstream_gene_variant | MODIFIER | c.*1687C>T| |
S294 |
13 | BAA06g13990 | A06 | 6917169 | G | A | downstream_gene_variant | MODIFIER | c.*2387G>A| |
S160 |
14 | BAA06g13990 | A06 | 6917462 | C | T | downstream_gene_variant | MODIFIER | c.*2680C>T| |
S148 S210 S30 S31 |
15 | BAA06g13990 | A06 | 6917920 | A | G | downstream_gene_variant | MODIFIER | c.*3138A>G| |
S43 |