Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g11450 | A08 | 10156093 | G | A | missense_variant | MODERATE | c.1825C>T|p.Arg609Trp |
S108 |
2 | BAA08g11450 | A08 | 10156942 | G | A | intron_variant | MODIFIER | c.1525+269C>T| |
S280 |
3 | BAA08g11450 | A08 | 10157244 | C | T | missense_variant | MODERATE | c.1492G>A|p.Asp498Asn |
S209 |
4 | BAA08g11450 | A08 | 10157295 | C | T | missense_variant | MODERATE | c.1441G>A|p.Gly481Arg |
S153 S213 |
5 | BAA08g11450 | A08 | 10157726 | T | C | missense_variant | MODERATE | c.1010A>G|p.Gln337Arg |
S125 |
6 | BAA08g11450 | A08 | 10158287 | G | A | missense_variant | MODERATE | c.661C>T|p.Pro221Ser |
S297 |
7 | BAA08g11450 | A08 | 10159134 | C | T | upstream_gene_variant | MODIFIER | c.-187G>A| |
S162 S31 |
8 | BAA08g11450 | A08 | 10161032 | C | T | upstream_gene_variant | MODIFIER | c.-2085G>A| |
S283 |
9 | BAA08g11450 | A08 | 10161470 | G | A | upstream_gene_variant | MODIFIER | c.-2523C>T| |
S204 |
10 | BAA08g11450 | A08 | 10161910 | G | A | upstream_gene_variant | MODIFIER | c.-2963C>T| |
S125 |
11 | BAA08g11450 | A08 | 10162030 | G | A | upstream_gene_variant | MODIFIER | c.-3083C>T| |
S146 |
12 | BAA08g11450 | A08 | 10162282 | C | T | upstream_gene_variant | MODIFIER | c.-3335G>A| |
S36 |
13 | BAA08g11450 | A08 | 10163089 | C | T | upstream_gene_variant | MODIFIER | c.-4142G>A| |
S249 |
14 | BAA08g11450 | A08 | 10163457 | C | T | upstream_gene_variant | MODIFIER | c.-4510G>A| |
S104 S52 |
15 | BAA08g11450 | A08 | 10163812 | C | T | upstream_gene_variant | MODIFIER | c.-4865G>A| |
S233 |