Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g13620 | A07 | 21462781 | G | A | missense_variant | MODERATE | c.4552C>T|p.Leu1518Phe |
S264 |
2 | BAA07g13620 | A07 | 21464377 | G | A | missense_variant | MODERATE | c.3746C>T|p.Ser1249Phe |
S281 |
3 | BAA07g13620 | A07 | 21464462 | C | T | missense_variant | MODERATE | c.3661G>A|p.Asp1221Asn |
S198 |
4 | BAA07g13620 | A07 | 21464766 | C | T | synonymous_variant | LOW | c.3357G>A|p.Lys1119Lys |
S100 |
5 | BAA07g13620 | A07 | 21467198 | G | A | stop_gained | HIGH | c.2089C>T|p.Gln697* |
S112 |
6 | BAA07g13620 | A07 | 21467590 | G | A | missense_variant | MODERATE | c.1841C>T|p.Ser614Phe |
S302 |
7 | BAA07g13620 | A07 | 21467942 | C | T | missense_variant | MODERATE | c.1564G>A|p.Asp522Asn |
S261 |
8 | BAA07g13620 | A07 | 21468274 | G | A | splice_region_variant&intron_variant | LOW | c.1307-3C>T| |
S92 |
9 | BAA07g13620 | A07 | 21468745 | G | A | synonymous_variant | LOW | c.918C>T|p.Leu306Leu |
S292 |
10 | BAA07g13620 | A07 | 21470076 | G | A | upstream_gene_variant | MODIFIER | c.-186C>T| |
S228 |
11 | BAA07g13620 | A07 | 21470711 | C | T | upstream_gene_variant | MODIFIER | c.-821G>A| |
S47 |
12 | BAA07g13620 | A07 | 21471437 | G | A | upstream_gene_variant | MODIFIER | c.-1547C>T| |
S190 |
13 | BAA07g13620 | A07 | 21472765 | G | A | upstream_gene_variant | MODIFIER | c.-2875C>T| |
S282 |
14 | BAA07g13620 | A07 | 21473013 | G | A | upstream_gene_variant | MODIFIER | c.-3123C>T| |
S40 S49 |
15 | BAA07g13620 | A07 | 21474721 | C | T | upstream_gene_variant | MODIFIER | c.-4831G>A| |
S20 |