Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12220 | A10 | 13662720 | C | T | synonymous_variant | LOW | c.3474G>A|p.Gln1158Gln |
S170 |
2 | BAA10g12220 | A10 | 13662776 | C | T | missense_variant | MODERATE | c.3418G>A|p.Asp1140Asn |
S260 |
3 | BAA10g12220 | A10 | 13662877 | C | T | missense_variant | MODERATE | c.3317G>A|p.Gly1106Glu |
S67 |
4 | BAA10g12220 | A10 | 13663165 | C | T | synonymous_variant | LOW | c.3105G>A|p.Lys1035Lys |
S238 |
5 | BAA10g12220 | A10 | 13663276 | C | T | synonymous_variant | LOW | c.2994G>A|p.Gln998Gln |
S42 |
6 | BAA10g12220 | A10 | 13665106 | C | T | missense_variant&splice_region_variant | MODERATE | c.1813G>A|p.Glu605Lys |
S61 |
7 | BAA10g12220 | A10 | 13665615 | C | T | missense_variant | MODERATE | c.1492G>A|p.Glu498Lys |
S124 |
8 | BAA10g12220 | A10 | 13667437 | G | A | intron_variant | MODIFIER | c.556-43C>T| |
S125 |
9 | BAA10g12220 | A10 | 13667616 | G | A | intron_variant | MODIFIER | c.454-23C>T| |
S151 S263 |
10 | BAA10g12220 | A10 | 13667937 | C | T | missense_variant | MODERATE | c.358G>A|p.Glu120Lys |
S42 S70 |
11 | BAA10g12220 | A10 | 13670281 | C | T | upstream_gene_variant | MODIFIER | c.-1987G>A| |
S143 |
12 | BAA10g12220 | A10 | 13670384 | C | T | upstream_gene_variant | MODIFIER | c.-2090G>A| |
S8 |
13 | BAA10g12220 | A10 | 13671154 | G | A | upstream_gene_variant | MODIFIER | c.-2860C>T| |
S172 S217 |
14 | BAA10g12220 | A10 | 13672336 | G | A | upstream_gene_variant | MODIFIER | c.-4042C>T| |
S126 |
15 | BAA10g12220 | A10 | 13673059 | C | T | upstream_gene_variant | MODIFIER | c.-4765G>A| |
S252 |