Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g10770 | A07 | 19627983 | G | A | downstream_gene_variant | MODIFIER | c.*2002C>T| |
S202 |
2 | BAA07g10770 | A07 | 19628481 | C | T | downstream_gene_variant | MODIFIER | c.*1504G>A| |
S12 |
3 | BAA07g10770 | A07 | 19629343 | G | A | downstream_gene_variant | MODIFIER | c.*642C>T| |
S228 |
4 | BAA07g10770 | A07 | 19629373 | C | T | downstream_gene_variant | MODIFIER | c.*612G>A| |
S75 S81 |
5 | BAA07g10770 | A07 | 19630299 | C | T | missense_variant | MODERATE | c.1231G>A|p.Gly411Arg |
S52 |
6 | BAA07g10770 | A07 | 19630652 | G | A | missense_variant | MODERATE | c.878C>T|p.Thr293Met |
S262 |
7 | BAA07g10770 | A07 | 19630671 | C | T | missense_variant | MODERATE | c.859G>A|p.Gly287Arg |
S13 |
8 | BAA07g10770 | A07 | 19630993 | G | A | synonymous_variant | LOW | c.537C>T|p.Asp179Asp |
S2 |
9 | BAA07g10770 | A07 | 19631031 | C | T | missense_variant | MODERATE | c.499G>A|p.Asp167Asn |
S152 |
10 | BAA07g10770 | A07 | 19631180 | C | T | missense_variant | MODERATE | c.350G>A|p.Gly117Glu |
S281 |
11 | BAA07g10770 | A07 | 19631279 | G | A | missense_variant | MODERATE | c.251C>T|p.Ser84Phe |
S39 |
12 | BAA07g10770 | A07 | 19631846 | G | A | upstream_gene_variant | MODIFIER | c.-317C>T| |
S112 |
13 | BAA07g10770 | A07 | 19631987 | C | T | upstream_gene_variant | MODIFIER | c.-458G>A| |
S229 |
14 | BAA07g10770 | A07 | 19633955 | G | A | upstream_gene_variant | MODIFIER | c.-2426C>T| |
S262 |
15 | BAA07g10770 | A07 | 19635007 | G | A | upstream_gene_variant | MODIFIER | c.-3478C>T| |
S238 |