Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02740 | A10 | 1307793 | G | A | upstream_gene_variant | MODIFIER | c.-4745G>A| |
S262 |
2 | BAA10g02740 | A10 | 1307983 | G | A | upstream_gene_variant | MODIFIER | c.-4555G>A| |
S13 |
3 | BAA10g02740 | A10 | 1308783 | C | T | upstream_gene_variant | MODIFIER | c.-3755C>T| |
S206 S26 |
4 | BAA10g02740 | A10 | 1309298 | C | T | upstream_gene_variant | MODIFIER | c.-3240C>T| |
S35 |
5 | BAA10g02740 | A10 | 1309747 | G | A | upstream_gene_variant | MODIFIER | c.-2791G>A| |
S153 S213 |
6 | BAA10g02740 | A10 | 1309755 | C | T | upstream_gene_variant | MODIFIER | c.-2783C>T| |
S155 S211 |
7 | BAA10g02740 | A10 | 1310853 | G | A | upstream_gene_variant | MODIFIER | c.-1685G>A| |
S68 |
8 | BAA10g02740 | A10 | 1311075 | G | A | upstream_gene_variant | MODIFIER | c.-1463G>A| |
S111 |
9 | BAA10g02740 | A10 | 1312733 | G | A | missense_variant | MODERATE | c.196G>A|p.Asp66Asn |
S262 |
10 | BAA10g02740 | A10 | 1314629 | G | A | missense_variant | MODERATE | c.931G>A|p.Ala311Thr |
S12 |
11 | BAA10g02740 | A10 | 1315763 | G | A | splice_region_variant&intron_variant | LOW | c.1399-4G>A| |
S55 |
12 | BAA10g02740 | A10 | 1315827 | G | A | missense_variant | MODERATE | c.1459G>A|p.Glu487Lys |
S187 |
13 | BAA10g02740 | A10 | 1316116 | C | T | missense_variant | MODERATE | c.1630C>T|p.Pro544Ser |
S269 |