Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g14190 | A08 | 12135082 | G | A | missense_variant | MODERATE | c.1871C>T|p.Pro624Leu |
S122 |
2 | BAA08g14190 | A08 | 12135997 | G | A | missense_variant&splice_region_variant | MODERATE | c.1417C>T|p.Pro473Ser |
S4 |
3 | BAA08g14190 | A08 | 12137412 | A | T | intron_variant | MODIFIER | c.1089-842T>A| |
S66 |
4 | BAA08g14190 | A08 | 12137647 | G | A | intron_variant | MODIFIER | c.1088+852C>T| |
S229 |
5 | BAA08g14190 | A08 | 12138530 | C | T | missense_variant | MODERATE | c.1057G>A|p.Val353Ile |
S219 |
6 | BAA08g14190 | A08 | 12138900 | C | T | missense_variant | MODERATE | c.770G>A|p.Ser257Asn |
S303 |
7 | BAA08g14190 | A08 | 12140256 | G | A | intron_variant | MODIFIER | c.471-1057C>T| |
S280 |
8 | BAA08g14190 | A08 | 12144849 | G | A | upstream_gene_variant | MODIFIER | c.-159C>T| |
S238 |
9 | BAA08g14190 | A08 | 12145110 | C | T | upstream_gene_variant | MODIFIER | c.-420G>A| |
S76 |
10 | BAA08g14190 | A08 | 12145430 | G | A | upstream_gene_variant | MODIFIER | c.-740C>T| |
S8 |
11 | BAA08g14190 | A08 | 12145518 | C | T | upstream_gene_variant | MODIFIER | c.-828G>A| |
S184 |
12 | BAA08g14190 | A08 | 12146178 | C | T | upstream_gene_variant | MODIFIER | c.-1488G>A| |
S47 |
13 | BAA08g14190 | A08 | 12149181 | G | A | upstream_gene_variant | MODIFIER | c.-4491C>T| |
S266 |