Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03420 | A10 | 1653753 | C | T | missense_variant | MODERATE | c.4246G>A|p.Glu1416Lys |
S37 |
2 | BAA10g03420 | A10 | 1653813 | C | T | missense_variant | MODERATE | c.4186G>A|p.Glu1396Lys |
S115 |
3 | BAA10g03420 | A10 | 1656137 | C | T | missense_variant | MODERATE | c.2657G>A|p.Arg886His |
S142 |
4 | BAA10g03420 | A10 | 1656911 | C | T | missense_variant | MODERATE | c.2183G>A|p.Arg728Lys |
S171 |
5 | BAA10g03420 | A10 | 1658758 | C | T | missense_variant | MODERATE | c.1468G>A|p.Val490Ile |
S152 |
6 | BAA10g03420 | A10 | 1659938 | C | T | missense_variant | MODERATE | c.1085G>A|p.Gly362Glu |
S286 |
7 | BAA10g03420 | A10 | 1660355 | C | T | missense_variant | MODERATE | c.787G>A|p.Glu263Lys |
S2 |
8 | BAA10g03420 | A10 | 1661226 | A | C | missense_variant | MODERATE | c.383T>G|p.Ile128Ser |
S137 S305 S9 S91 |
9 | BAA10g03420 | A10 | 1661404 | G | A | missense_variant | MODERATE | c.205C>T|p.Pro69Ser |
S296 |
10 | BAA10g03420 | A10 | 1661624 | G | A | upstream_gene_variant | MODIFIER | c.-16C>T| |
S245 |
11 | BAA10g03420 | A10 | 1662260 | G | A | upstream_gene_variant | MODIFIER | c.-652C>T| |
S230 |
12 | BAA10g03420 | A10 | 1664284 | C | T | upstream_gene_variant | MODIFIER | c.-2676G>A| |
S203 |
13 | BAA10g03420 | A10 | 1664611 | C | T | upstream_gene_variant | MODIFIER | c.-3003G>A| |
S10 |
14 | BAA10g03420 | A10 | 1665076 | C | T | upstream_gene_variant | MODIFIER | c.-3468G>A| |
S291 |
15 | BAA10g03420 | A10 | 1665222 | G | A | upstream_gene_variant | MODIFIER | c.-3614C>T| |
S69 |
16 | BAA10g03420 | A10 | 1665315 | C | T | upstream_gene_variant | MODIFIER | c.-3707G>A| |
S177 |
17 | BAA10g03420 | A10 | 1665500 | C | T | upstream_gene_variant | MODIFIER | c.-3892G>A| |
S308 |
18 | BAA10g03420 | A10 | 1665593 | C | T | upstream_gene_variant | MODIFIER | c.-3985G>A| |
S142 |
19 | BAA10g03420 | A10 | 1666047 | C | T | upstream_gene_variant | MODIFIER | c.-4439G>A| |
S23 |