Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g10770 | A06 | 5422312 | C | T | upstream_gene_variant | MODIFIER | c.-347C>T| |
S301 S304 |
2 | BAA06g10770 | A06 | 5422357 | C | T | upstream_gene_variant | MODIFIER | c.-302C>T| |
S1 |
3 | BAA06g10770 | A06 | 5422361 | G | A | upstream_gene_variant | MODIFIER | c.-298G>A| |
S210 |
4 | BAA06g10770 | A06 | 5423269 | G | A | missense_variant | MODERATE | c.611G>A|p.Gly204Asp |
S35 |
5 | BAA06g10770 | A06 | 5424737 | G | A | synonymous_variant | LOW | c.1755G>A|p.Gly585Gly |
S64 |
6 | BAA06g10770 | A06 | 5425266 | C | T | missense_variant | MODERATE | c.2284C>T|p.Arg762Cys |
S98 |
7 | BAA06g10770 | A06 | 5425382 | C | T | synonymous_variant | LOW | c.2400C>T|p.Ala800Ala |
S303 |
8 | BAA06g10770 | A06 | 5425635 | G | A | missense_variant | MODERATE | c.2653G>A|p.Asp885Asn |
S42 |
9 | BAA06g10770 | A06 | 5425952 | C | T | synonymous_variant | LOW | c.2970C>T|p.His990His |
S150 |
10 | BAA06g10770 | A06 | 5426061 | C | T | missense_variant | MODERATE | c.3079C>T|p.Pro1027Ser |
S74 |
11 | BAA06g10770 | A06 | 5426290 | G | A | missense_variant | MODERATE | c.3308G>A|p.Arg1103Lys |
S149 |
12 | BAA06g10770 | A06 | 5426520 | C | T | missense_variant | MODERATE | c.3538C>T|p.Pro1180Ser |
S279 |
13 | BAA06g10770 | A06 | 5426661 | G | A | missense_variant | MODERATE | c.3679G>A|p.Glu1227Lys |
S249 |
14 | BAA06g10770 | A06 | 5426907 | G | A | missense_variant | MODERATE | c.3925G>A|p.Gly1309Arg |
S77 S82 |
15 | BAA06g10770 | A06 | 5430449 | G | A | downstream_gene_variant | MODIFIER | c.*3120G>A| |
S284 |
16 | BAA06g10770 | A06 | 5431027 | C | T | downstream_gene_variant | MODIFIER | c.*3698C>T| |
S302 |
17 | BAA06g10770 | A06 | 5432105 | C | T | downstream_gene_variant | MODIFIER | c.*4776C>T| |
S164 |